Canonical Allele Identifier: CA803465702

Gene: ALDH7A1

Linked Data

• dbSNP Id: rs1192975179
• gnomAD v3: 5-126568230-AAAATCCTC-A
• gnomAD v4: 5-126568230-AAAATCCTC-A
• MyVariant Identifiers: chr5:g.125903923_125903930del (hg19) ; chr5:g.126568231_126568238del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126568232_126568239del , CM000667.2:g.126568232_126568239del	GRCh38
NC_000005.9:g.125903924_125903931del , CM000667.1:g.125903924_125903931del	GRCh37
NC_000005.8:g.125931823_125931830del	NCBI36
NG_008600.2:g.32153_32160del
NG_008600.3:g.32153_32160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.871+21_871+28del MANE Select	ENSP00000387123.3:n.871+21_871+28del
ENST00000413020.6:c.871+21_871+28del	ENSP00000487936.1:n.871+21_871+28del
ENST00000458249.6:c.*780+21_*780+28del	ENSP00000403929.1:n.*780+21_*780+28del
ENST00000503281.6:c.460+21_460+28del
ENST00000509459.6:c.419+21_419+28del
ENST00000511266.6:n.1614_1621del
ENST00000635851.1:c.869+21_869+28del
ENST00000636062.1:n.766+21_766+28del
ENST00000636225.1:c.*680+21_*680+28del	ENSP00000490797.1:n.*680+21_*680+28del
ENST00000636286.1:n.589+21_589+28del
ENST00000636743.1:c.751+21_751+28del	ENSP00000489725.1:n.751+21_751+28del
ENST00000636808.1:c.*680+21_*680+28del	ENSP00000490833.1:n.*680+21_*680+28del
ENST00000636872.1:c.1031+21_1031+28del	ENSP00000490919.1:n.1031+21_1031+28del
ENST00000636879.1:c.916+21_916+28del	ENSP00000490811.1:n.916+21_916+28del
ENST00000636886.1:c.670+21_670+28del	ENSP00000490371.1:n.670+21_670+28del
ENST00000636892.1:n.2900_2907del
ENST00000637206.1:c.871+21_871+28del	ENSP00000489895.1:n.871+21_871+28del
ENST00000637272.1:c.871+21_871+28del	ENSP00000489686.1:n.871+21_871+28del
ENST00000637292.1:c.426+2544_426+2551del
ENST00000637782.1:c.871+21_871+28del	ENSP00000490024.1:n.871+21_871+28del
ENST00000637964.1:c.817+21_817+28del	ENSP00000490291.1:n.817+21_817+28del
ENST00000638008.1:c.*715+2544_*715+2551del	ENSP00000490400.1:n.*715+2544_*715+2551del
ENST00000409134.7:c.871+21_871+28del	ENSP00000387123.3:n.871+21_871+28del
ENST00000413020.5:c.871+21_871+28del	ENSP00000487936.1:n.871+21_871+28del
ENST00000433026.5:n.398+21_398+28del
ENST00000447989.6:c.952+21_952+28del	ENSP00000414132.2:n.952+21_952+28del
ENST00000503281.5:c.460+21_460+28del
ENST00000509459.5:c.419+21_419+28del
ENST00000553117.5:c.871+21_871+28del	ENSP00000448593.1:n.871+21_871+28del
NM_001182.4:c.871+21_871+28del	NP_001173.2:n.871+21_871+28del
NM_001201377.1:c.787+21_787+28del	NP_001188306.1:n.787+21_787+28del
NM_001202404.1:c.952+21_952+28del	NP_001189333.1:n.952+21_952+28del
XM_011543417.1:c.466+21_466+28del	XP_011541719.1:n.466+21_466+28del
XM_011543417.2:c.466+21_466+28del	XP_011541719.1:n.466+21_466+28del
NM_001182.5:c.871+21_871+28del MANE Select	NP_001173.2:n.871+21_871+28del
NM_001201377.2:c.787+21_787+28del	NP_001188306.1:n.787+21_787+28del
NM_001202404.2:c.871+21_871+28del	NP_001189333.2:n.871+21_871+28del