Canonical Allele Identifier: CA2541351134

Gene: ALDH7A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126545292_126545293insTC , CM000667.2:g.126545292_126545293insTC	GRCh38
NC_000005.9:g.125880984_125880985insTC , CM000667.1:g.125880984_125880985insTC	GRCh37
NC_000005.8:g.125908883_125908884insTC	NCBI36
NG_008600.2:g.55098_55099insGA
NG_008600.3:g.55098_55099insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409134.8:c.1566-274_1566-273insGA MANE Select	ENSP00000387123.3:n.1566-274_1566-273insGA
ENST00000458249.6:c.*1475-274_*1475-273insGA	ENSP00000403929.1:n.*1475-274_*1475-273insGA
ENST00000485852.7:n.313-274_313-273insGA
ENST00000497231.7:n.1993-274_1993-273insGA
ENST00000635851.1:c.1563+1031_1563+1032insGA
ENST00000636286.1:n.1331-274_1331-273insGA
ENST00000636482.1:n.1100-274_1100-273insGA
ENST00000636743.1:c.1446-274_1446-273insGA	ENSP00000489725.1:n.1446-274_1446-273insGA
ENST00000636808.1:c.*1375-274_*1375-273insGA	ENSP00000490833.1:n.*1375-274_*1375-273insGA
ENST00000636872.1:c.1726-274_1726-273insGA	ENSP00000490919.1:n.1726-274_1726-273insGA
ENST00000636879.1:c.1611-274_1611-273insGA	ENSP00000490811.1:n.1611-274_1611-273insGA
ENST00000636886.1:c.1365-274_1365-273insGA	ENSP00000490371.1:n.1365-274_1365-273insGA
ENST00000637206.1:c.1386-274_1386-273insGA	ENSP00000489895.1:n.1386-274_1386-273insGA
ENST00000637272.1:c.1557-274_1557-273insGA	ENSP00000489686.1:n.1557-274_1557-273insGA
ENST00000637292.1:c.1022-274_1022-273insGA
ENST00000637782.1:c.1565+1031_1565+1032insGA	ENSP00000490024.1:n.1565+1031_1565+1032insGA
ENST00000638008.1:c.*1410-274_*1410-273insGA	ENSP00000490400.1:n.*1410-274_*1410-273insGA
ENST00000638010.1:n.1512-274_1512-273insGA
ENST00000409134.7:c.1566-274_1566-273insGA	ENSP00000387123.3:n.1566-274_1566-273insGA
ENST00000447989.6:c.1455-274_1455-273insGA	ENSP00000414132.2:n.1455-274_1455-273insGA
ENST00000485852.6:n.313-274_313-273insGA
ENST00000497231.6:n.1776-274_1776-273insGA
ENST00000553117.5:c.1374-274_1374-273insGA	ENSP00000448593.1:n.1374-274_1374-273insGA
NM_001182.4:c.1566-274_1566-273insGA	NP_001173.2:n.1566-274_1566-273insGA
NM_001201377.1:c.1482-274_1482-273insGA	NP_001188306.1:n.1482-274_1482-273insGA
NM_001202404.1:c.1455-274_1455-273insGA	NP_001189333.1:n.1455-274_1455-273insGA
XM_011543417.1:c.1161-274_1161-273insGA	XP_011541719.1:n.1161-274_1161-273insGA
XM_011543417.2:c.1161-274_1161-273insGA	XP_011541719.1:n.1161-274_1161-273insGA
NM_001182.5:c.1566-274_1566-273insGA MANE Select	NP_001173.2:n.1566-274_1566-273insGA
NM_001201377.2:c.1482-274_1482-273insGA	NP_001188306.1:n.1482-274_1482-273insGA
NM_001202404.2:c.1374-274_1374-273insGA	NP_001189333.2:n.1374-274_1374-273insGA