Canonical Allele Identifier: CA360717875
Gene: ALDH7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126545007G>C , CM000667.2:g.126545007G>C GRCh38
NC_000005.9:g.125880699G>C , CM000667.1:g.125880699G>C GRCh37
NC_000005.8:g.125908598G>C NCBI36
NG_008600.2:g.55384C>G
NG_008600.3:g.55384C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409134.8:c.1578C>G MANE Select ENSP00000387123.3:p.Tyr526Ter
ENST00000458249.6:c.*1487C>G ENSP00000403929.1:n.*1487C>G
ENST00000485852.7:n.325C>G
ENST00000497231.7:n.2005C>G
ENST00000635851.1:c.1563+1317C>G
ENST00000636286.1:n.1343C>G
ENST00000636482.1:n.1112C>G
ENST00000636743.1:c.1458C>G ENSP00000489725.1:p.Tyr486Ter
ENST00000636808.1:c.*1387C>G ENSP00000490833.1:n.*1387C>G
ENST00000636872.1:c.1738C>G ENSP00000490919.1:n.1738C>G
ENST00000636879.1:c.1623C>G ENSP00000490811.1:p.Tyr541Ter
ENST00000636886.1:c.1377C>G ENSP00000490371.1:p.Tyr459Ter
ENST00000637206.1:c.1398C>G ENSP00000489895.1:p.Tyr466Ter
ENST00000637272.1:c.1569C>G ENSP00000489686.1:p.Tyr523Ter
ENST00000637292.1:c.1034C>G
ENST00000637782.1:c.1565+1317C>G ENSP00000490024.1:n.1565+1317C>G
ENST00000638008.1:c.*1422C>G ENSP00000490400.1:n.*1422C>G
ENST00000638010.1:n.1524C>G
ENST00000409134.7:c.1578C>G ENSP00000387123.3:p.Tyr526Ter
ENST00000447989.6:c.1467C>G ENSP00000414132.2:p.Tyr489Ter
ENST00000485852.6:n.325C>G
ENST00000497231.6:n.1788C>G
ENST00000553117.5:c.1386C>G ENSP00000448593.1:p.Tyr462Ter
NM_001182.4:c.1578C>G NP_001173.2:p.Tyr526Ter
NM_001201377.1:c.1494C>G NP_001188306.1:p.Tyr498Ter
NM_001202404.1:c.1467C>G NP_001189333.1:p.Tyr489Ter
XM_011543417.1:c.1173C>G XP_011541719.1:p.Tyr391Ter
XM_011543417.2:c.1173C>G XP_011541719.1:p.Tyr391Ter
NM_001182.5:c.1578C>G MANE Select NP_001173.2:p.Tyr526Ter
NM_001201377.2:c.1494C>G NP_001188306.1:p.Tyr498Ter
NM_001202404.2:c.1386C>G NP_001189333.2:p.Tyr462Ter