Canonical Allele Identifier: CA1768019862
Gene: ASAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18061377C= , CM000670.2:g.18061377C= GRCh38
NC_000008.10:g.17918886C= , CM000670.1:g.17918886C= GRCh37
NC_000008.9:g.17963166C= NCBI36
NG_008985.1:g.28622G=
NG_008985.2:g.28622G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381733.9:c.833G= ENSP00000371152.4:p.Ser278=
ENST00000518746.2:n.2471G=
ENST00000520781.6:c.710G= ENSP00000427751.1:p.Ser237=
ENST00000521542.2:n.93G=
ENST00000635756.1:c.198G=
ENST00000635944.1:c.*621G= ENSP00000490195.1:n.*621G=
ENST00000635998.1:c.785G= ENSP00000490506.1:p.Ser262=
ENST00000636009.1:c.642G= ENSP00000489988.1:n.642G=
ENST00000636033.1:c.*621G= ENSP00000489617.1:n.*621G=
ENST00000636050.1:c.*628G= ENSP00000490562.1:n.*628G=
ENST00000636128.1:c.464G= ENSP00000489789.1:p.Ser155=
ENST00000636160.1:c.*677G= ENSP00000489651.1:n.*677G=
ENST00000636171.1:c.728G= ENSP00000489761.1:p.Ser243=
ENST00000636455.1:c.833G= ENSP00000490502.1:p.Ser278=
ENST00000636494.1:c.*565G= ENSP00000490388.1:n.*565G=
ENST00000636563.1:n.447G=
ENST00000636577.1:c.725G= ENSP00000490027.1:p.Ser242=
ENST00000636691.1:c.590G= ENSP00000490725.1:p.Ser197=
ENST00000636701.1:c.*436G= ENSP00000489800.1:n.*436G=
ENST00000636815.1:c.702G=
ENST00000636920.1:c.*621G= ENSP00000490437.1:n.*621G=
ENST00000636997.1:c.698G= ENSP00000490093.1:p.Ser233=
ENST00000637013.1:c.*1153G= ENSP00000490596.1:n.*1153G=
ENST00000637014.1:n.1192G=
ENST00000637095.1:c.*565G= ENSP00000490415.1:n.*565G=
ENST00000637244.1:c.*1303G= ENSP00000490188.1:n.*1303G=
ENST00000637343.1:n.2222G=
ENST00000637429.1:c.*997G= ENSP00000490522.1:n.*997G=
ENST00000637484.1:c.*747G= ENSP00000490837.1:n.*747G=
ENST00000637528.1:c.722G= ENSP00000490801.1:p.Ser241=
ENST00000637609.1:n.3506G=
ENST00000637636.1:c.779G= ENSP00000490112.1:p.Ser260=
ENST00000637790.2:c.785G= MANE Select ENSP00000490272.1:p.Ser262=
ENST00000637857.1:n.1151G=
ENST00000637922.1:c.590G= ENSP00000490071.1:p.Ser197=
ENST00000637991.1:c.758G= ENSP00000489901.1:p.Ser253=
ENST00000638028.1:n.1002G=
ENST00000638069.1:n.1606G=
ENST00000262097.10:c.785G= ENSP00000262097.6:p.Ser262=
ENST00000314146.10:c.767G= ENSP00000326970.10:p.Ser256=
ENST00000381733.8:c.833G= ENSP00000371152.4:p.Ser278=
ENST00000519468.5:n.614G=
ENST00000520781.5:c.710G= ENSP00000427751.1:p.Ser237=
ENST00000521542.1:n.498G=
NM_001127505.1:c.767G= NP_001120977.1:p.Ser256=
NM_001127505.2:c.767G= NP_001120977.1:p.Ser256=
NM_004315.4:c.833G= NP_004306.3:p.Ser278=
NM_004315.5:c.833G= NP_004306.3:p.Ser278=
NM_177924.3:c.785G= NP_808592.2:p.Ser262=
NM_177924.4:c.785G= NP_808592.2:p.Ser262=
XM_005273504.2:c.719G= XP_005273561.1:p.Ser240=
NM_001363743.1:c.590G= NP_001350672.1:p.Ser197=
XM_005273504.3:c.719G= XP_005273561.1:p.Ser240=
NM_177924.5:c.785G= MANE Select NP_808592.2:p.Ser262=
NM_001127505.3:c.767G= NP_001120977.1:p.Ser256=
NM_001363743.2:c.590G= NP_001350672.1:p.Ser197=
NM_004315.6:c.833G= NP_004306.3:p.Ser278=