Canonical Allele Identifier: CA1768019744
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18061324_18061326delinsAAT , CM000670.2:g.18061324_18061326delinsAAT GRCh38
NC_000008.10:g.17918833_17918835delinsAAT , CM000670.1:g.17918833_17918835delinsAAT GRCh37
NC_000008.9:g.17963113_17963115delinsAAT NCBI36
NG_008985.1:g.28673_28675delinsATT
NG_008985.2:g.28673_28675delinsATT

Transcript Alleles

HGVS Amino-acid change
ENST00000381733.9:c.833+51_833+53delinsATT ENSP00000371152.4:n.833+51_833+53delinsAT...
ENST00000518746.2:n.2471+51_2471+53delinsATT
ENST00000520781.6:c.710+51_710+53delinsATT ENSP00000427751.1:n.710+51_710+53delinsAT...
ENST00000521542.2:n.144_146delinsATT
ENST00000635756.1:c.198+51_198+53delinsATT
ENST00000635944.1:c.*621+51_*621+53delinsATT ENSP00000490195.1:n.*621+51_*621+53delins...
ENST00000635998.1:c.785+51_785+53delinsATT ENSP00000490506.1:n.785+51_785+53delinsAT...
ENST00000636009.1:c.642+51_642+53delinsATT ENSP00000489988.1:n.642+51_642+53delinsAT...
ENST00000636033.1:c.*621+51_*621+53delinsATT ENSP00000489617.1:n.*621+51_*621+53delins...
ENST00000636050.1:c.*628+51_*628+53delinsATT ENSP00000490562.1:n.*628+51_*628+53delins...
ENST00000636128.1:c.464+51_464+53delinsATT ENSP00000489789.1:n.464+51_464+53delinsAT...
ENST00000636160.1:c.*677+51_*677+53delinsATT ENSP00000489651.1:n.*677+51_*677+53delins...
ENST00000636171.1:c.728+51_728+53delinsATT ENSP00000489761.1:n.728+51_728+53delinsAT...
ENST00000636455.1:c.833+51_833+53delinsATT ENSP00000490502.1:n.833+51_833+53delinsAT...
ENST00000636494.1:c.*565+51_*565+53delinsATT ENSP00000490388.1:n.*565+51_*565+53delins...
ENST00000636563.1:n.447+51_447+53delinsATT
ENST00000636577.1:c.725+51_725+53delinsATT ENSP00000490027.1:n.725+51_725+53delinsAT...
ENST00000636691.1:c.590+51_590+53delinsATT ENSP00000490725.1:n.590+51_590+53delinsAT...
ENST00000636701.1:c.*436+51_*436+53delinsATT ENSP00000489800.1:n.*436+51_*436+53delins...
ENST00000636815.1:c.702+51_702+53delinsATT
ENST00000636920.1:c.*621+51_*621+53delinsATT ENSP00000490437.1:n.*621+51_*621+53delins...
ENST00000636997.1:c.698+51_698+53delinsATT ENSP00000490093.1:n.698+51_698+53delinsAT...
ENST00000637013.1:c.*1153+51_*1153+53delinsATT ENSP00000490596.1:n.*1153+51_*1153+53deli...
ENST00000637014.1:n.1192+51_1192+53delinsATT
ENST00000637095.1:c.*565+51_*565+53delinsATT ENSP00000490415.1:n.*565+51_*565+53delins...
ENST00000637244.1:c.*1303+51_*1303+53delinsATT ENSP00000490188.1:n.*1303+51_*1303+53deli...
ENST00000637343.1:n.2222+51_2222+53delinsATT
ENST00000637429.1:c.*997+51_*997+53delinsATT ENSP00000490522.1:n.*997+51_*997+53delins...
ENST00000637484.1:c.*747+51_*747+53delinsATT ENSP00000490837.1:n.*747+51_*747+53delins...
ENST00000637528.1:c.722+51_722+53delinsATT ENSP00000490801.1:n.722+51_722+53delinsAT...
ENST00000637609.1:n.3506+51_3506+53delinsATT
ENST00000637636.1:c.779+51_779+53delinsATT ENSP00000490112.1:n.779+51_779+53delinsAT...
ENST00000637790.2:c.785+51_785+53delinsATT MANE Select ENSP00000490272.1:n.785+51_785+53delinsAT...
ENST00000637857.1:n.1151+51_1151+53delinsATT
ENST00000637922.1:c.590+51_590+53delinsATT ENSP00000490071.1:n.590+51_590+53delinsAT...
ENST00000637991.1:c.758+51_758+53delinsATT ENSP00000489901.1:n.758+51_758+53delinsAT...
ENST00000638028.1:n.1002+51_1002+53delinsATT
ENST00000638069.1:n.1606+51_1606+53delinsATT
ENST00000262097.10:c.785+51_785+53delinsATT ENSP00000262097.6:n.785+51_785+53delinsAT...
ENST00000314146.10:c.767+51_767+53delinsATT ENSP00000326970.10:n.767+51_767+53delinsA...
ENST00000381733.8:c.833+51_833+53delinsATT ENSP00000371152.4:n.833+51_833+53delinsAT...
ENST00000519468.5:n.614+51_614+53delinsATT
ENST00000520781.5:c.710+51_710+53delinsATT ENSP00000427751.1:n.710+51_710+53delinsAT...
ENST00000521542.1:n.498+51_498+53delinsATT
NM_001127505.1:c.767+51_767+53delinsATT NP_001120977.1:n.767+51_767+53delinsATT
NM_001127505.2:c.767+51_767+53delinsATT NP_001120977.1:n.767+51_767+53delinsATT
NM_004315.4:c.833+51_833+53delinsATT NP_004306.3:n.833+51_833+53delinsATT
NM_004315.5:c.833+51_833+53delinsATT NP_004306.3:n.833+51_833+53delinsATT
NM_177924.3:c.785+51_785+53delinsATT NP_808592.2:n.785+51_785+53delinsATT
NM_177924.4:c.785+51_785+53delinsATT NP_808592.2:n.785+51_785+53delinsATT
XM_005273504.2:c.719+51_719+53delinsATT XP_005273561.1:n.719+51_719+53delinsATT
NM_001363743.1:c.590+51_590+53delinsATT NP_001350672.1:n.590+51_590+53delinsATT
XM_005273504.3:c.719+51_719+53delinsATT XP_005273561.1:n.719+51_719+53delinsATT
NM_177924.5:c.785+51_785+53delinsATT MANE Select NP_808592.2:n.785+51_785+53delinsATT
NM_001127505.3:c.767+51_767+53delinsATT NP_001120977.1:n.767+51_767+53delinsATT
NM_001363743.2:c.590+51_590+53delinsATT NP_001350672.1:n.590+51_590+53delinsATT
NM_004315.6:c.833+51_833+53delinsATT NP_004306.3:n.833+51_833+53delinsATT