Canonical Allele Identifier: CA1480005061
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428309T= , CM000666.2:g.99428309T= GRCh38
NC_000004.11:g.100349466T= , CM000666.1:g.100349466T= GRCh37
NC_000004.10:g.100568489T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000673.7:c.260-135A= MANE Select NP_000664.3:n.260-135A=
ENST00000437033.7:c.260-135A= MANE Select ENSP00000414254.2:n.260-135A=
NM_000673.4:c.296-135A= NP_000664.2:n.296-135A=
NM_001166504.1:c.320-135A= NP_001159976.1:n.320-135A=
NM_001166504.2:c.320-135A= NP_001159976.1:n.320-135A=
ENST00000209665.8:c.296-135A= ENSP00000209665.4:n.296-135A=
ENST00000437033.6:c.260-135A= ENSP00000414254.2:n.260-135A=
ENST00000474027.1:c.89-135A= ENSP00000420300.1:n.89-135A=
ENST00000476959.5:c.320-135A= ENSP00000420269.1:n.320-135A=
ENST00000482593.5:c.89-135A= ENSP00000420613.1:n.89-135A=