Canonical Allele Identifier: CA1479994763

Gene: ADH7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420996_99421000delinsAAGAG , CM000666.2:g.99420996_99421000delinsAAGAG	GRCh38
NC_000004.11:g.100342153_100342157delinsAAGAG , CM000666.1:g.100342153_100342157delinsAAGAG	GRCh37
NC_000004.10:g.100561176_100561180delinsAAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.565-207_565-203delinsCTCTT MANE Select	ENSP00000414254.2:n.565-207_565-203delinsCTCTT
ENST00000209665.8:c.601-207_601-203delinsCTCTT	ENSP00000209665.4:n.601-207_601-203delinsCTCTT
ENST00000437033.6:c.565-207_565-203delinsCTCTT	ENSP00000414254.2:n.565-207_565-203delinsCTCTT
ENST00000476959.5:c.625-207_625-203delinsCTCTT	ENSP00000420269.1:n.625-207_625-203delinsCTCTT
ENST00000482593.5:c.394-207_394-203delinsCTCTT	ENSP00000420613.1:n.394-207_394-203delinsCTCTT
NM_000673.4:c.601-207_601-203delinsCTCTT	NP_000664.2:n.601-207_601-203delinsCTCTT
NM_001166504.1:c.625-207_625-203delinsCTCTT	NP_001159976.1:n.625-207_625-203delinsCTCTT
NM_000673.7:c.565-207_565-203delinsCTCTT MANE Select	NP_000664.3:n.565-207_565-203delinsCTCTT
NM_001166504.2:c.625-207_625-203delinsCTCTT	NP_001159976.1:n.625-207_625-203delinsCTCTT