Canonical Allele Identifier: CA2832612258

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126568245A>C , CM000667.2:g.126568245A>C	GRCh38
NC_000005.9:g.125903937A>C , CM000667.1:g.125903937A>C	GRCh37
NC_000005.8:g.125931836A>C	NCBI36
NG_008600.2:g.32146T>G
NG_008600.3:g.32146T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.871+14T>G MANE Select	ENSP00000387123.3:n.871+14T>G
ENST00000413020.6:c.871+14T>G	ENSP00000487936.1:n.871+14T>G
ENST00000458249.6:c.*780+14T>G	ENSP00000403929.1:n.*780+14T>G
ENST00000503281.6:c.460+14T>G
ENST00000509459.6:c.419+14T>G
ENST00000511266.6:n.1607T>G
ENST00000635851.1:c.869+14T>G
ENST00000636062.1:n.766+14T>G
ENST00000636225.1:c.*680+14T>G	ENSP00000490797.1:n.*680+14T>G
ENST00000636286.1:n.589+14T>G
ENST00000636743.1:c.751+14T>G	ENSP00000489725.1:n.751+14T>G
ENST00000636808.1:c.*680+14T>G	ENSP00000490833.1:n.*680+14T>G
ENST00000636872.1:c.1031+14T>G	ENSP00000490919.1:n.1031+14T>G
ENST00000636879.1:c.916+14T>G	ENSP00000490811.1:n.916+14T>G
ENST00000636886.1:c.670+14T>G	ENSP00000490371.1:n.670+14T>G
ENST00000636892.1:n.2893T>G
ENST00000637206.1:c.871+14T>G	ENSP00000489895.1:n.871+14T>G
ENST00000637272.1:c.871+14T>G	ENSP00000489686.1:n.871+14T>G
ENST00000637292.1:c.426+2537T>G
ENST00000637782.1:c.871+14T>G	ENSP00000490024.1:n.871+14T>G
ENST00000637964.1:c.817+14T>G	ENSP00000490291.1:n.817+14T>G
ENST00000638008.1:c.*715+2537T>G	ENSP00000490400.1:n.*715+2537T>G
ENST00000409134.7:c.871+14T>G	ENSP00000387123.3:n.871+14T>G
ENST00000413020.5:c.871+14T>G	ENSP00000487936.1:n.871+14T>G
ENST00000433026.5:n.398+14T>G
ENST00000447989.6:c.952+14T>G	ENSP00000414132.2:n.952+14T>G
ENST00000503281.5:c.460+14T>G
ENST00000509459.5:c.419+14T>G
ENST00000553117.5:c.871+14T>G	ENSP00000448593.1:n.871+14T>G
NM_001182.4:c.871+14T>G	NP_001173.2:n.871+14T>G
NM_001201377.1:c.787+14T>G	NP_001188306.1:n.787+14T>G
NM_001202404.1:c.952+14T>G	NP_001189333.1:n.952+14T>G
XM_011543417.1:c.466+14T>G	XP_011541719.1:n.466+14T>G
XM_011543417.2:c.466+14T>G	XP_011541719.1:n.466+14T>G
NM_001182.5:c.871+14T>G MANE Select	NP_001173.2:n.871+14T>G
NM_001201377.2:c.787+14T>G	NP_001188306.1:n.787+14T>G
NM_001202404.2:c.871+14T>G	NP_001189333.2:n.871+14T>G