Canonical Allele Identifier: CA126901784
Gene: ALDH7A1 HGNC NCBI

Linked Data

dbSNP Id: rs751019176

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126568235C>G , CM000667.2:g.126568235C>G GRCh38
NC_000005.9:g.125903927C>G , CM000667.1:g.125903927C>G GRCh37
NC_000005.8:g.125931826C>G NCBI36
NG_008600.2:g.32156G>C
NG_008600.3:g.32156G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.871+24G>C MANE Select ENSP00000387123.3:n.871+24G>C
ENST00000413020.6:c.871+24G>C ENSP00000487936.1:n.871+24G>C
ENST00000458249.6:c.*780+24G>C ENSP00000403929.1:n.*780+24G>C
ENST00000503281.6:c.460+24G>C
ENST00000509459.6:c.419+24G>C
ENST00000511266.6:n.1617G>C
ENST00000635851.1:c.869+24G>C
ENST00000636062.1:n.766+24G>C
ENST00000636225.1:c.*680+24G>C ENSP00000490797.1:n.*680+24G>C
ENST00000636286.1:n.589+24G>C
ENST00000636743.1:c.751+24G>C ENSP00000489725.1:n.751+24G>C
ENST00000636808.1:c.*680+24G>C ENSP00000490833.1:n.*680+24G>C
ENST00000636872.1:c.1031+24G>C ENSP00000490919.1:n.1031+24G>C
ENST00000636879.1:c.916+24G>C ENSP00000490811.1:n.916+24G>C
ENST00000636886.1:c.670+24G>C ENSP00000490371.1:n.670+24G>C
ENST00000636892.1:n.2903G>C
ENST00000637206.1:c.871+24G>C ENSP00000489895.1:n.871+24G>C
ENST00000637272.1:c.871+24G>C ENSP00000489686.1:n.871+24G>C
ENST00000637292.1:c.426+2547G>C
ENST00000637782.1:c.871+24G>C ENSP00000490024.1:n.871+24G>C
ENST00000637964.1:c.817+24G>C ENSP00000490291.1:n.817+24G>C
ENST00000638008.1:c.*715+2547G>C ENSP00000490400.1:n.*715+2547G>C
ENST00000409134.7:c.871+24G>C ENSP00000387123.3:n.871+24G>C
ENST00000413020.5:c.871+24G>C ENSP00000487936.1:n.871+24G>C
ENST00000433026.5:n.398+24G>C
ENST00000447989.6:c.952+24G>C ENSP00000414132.2:n.952+24G>C
ENST00000503281.5:c.460+24G>C
ENST00000509459.5:c.419+24G>C
ENST00000553117.5:c.871+24G>C ENSP00000448593.1:n.871+24G>C
NM_001182.4:c.871+24G>C NP_001173.2:n.871+24G>C
NM_001201377.1:c.787+24G>C NP_001188306.1:n.787+24G>C
NM_001202404.1:c.952+24G>C NP_001189333.1:n.952+24G>C
XM_011543417.1:c.466+24G>C XP_011541719.1:n.466+24G>C
XM_011543417.2:c.466+24G>C XP_011541719.1:n.466+24G>C
NM_001182.5:c.871+24G>C MANE Select NP_001173.2:n.871+24G>C
NM_001201377.2:c.787+24G>C NP_001188306.1:n.787+24G>C
NM_001202404.2:c.871+24G>C NP_001189333.2:n.871+24G>C