Canonical Allele Identifier: CA1479993748

Gene: ADH7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420523_99420524delinsTG , CM000666.2:g.99420523_99420524delinsTG	GRCh38
NC_000004.11:g.100341680_100341681delinsTG , CM000666.1:g.100341680_100341681delinsTG	GRCh37
NC_000004.10:g.100560703_100560704delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.825+9_825+10delinsCA MANE Select	ENSP00000414254.2:n.825+9_825+10delinsCA
ENST00000209665.8:c.861+9_861+10delinsCA	ENSP00000209665.4:n.861+9_861+10delinsCA
ENST00000437033.6:c.825+9_825+10delinsCA	ENSP00000414254.2:n.825+9_825+10delinsCA
ENST00000476959.5:c.885+9_885+10delinsCA	ENSP00000420269.1:n.885+9_885+10delinsCA
ENST00000482593.5:c.654+9_654+10delinsCA	ENSP00000420613.1:n.654+9_654+10delinsCA
NM_000673.4:c.861+9_861+10delinsCA	NP_000664.2:n.861+9_861+10delinsCA
NM_001166504.1:c.885+9_885+10delinsCA	NP_001159976.1:n.885+9_885+10delinsCA
NM_000673.7:c.825+9_825+10delinsCA MANE Select	NP_000664.3:n.825+9_825+10delinsCA
NM_001166504.2:c.885+9_885+10delinsCA	NP_001159976.1:n.885+9_885+10delinsCA