Canonical Allele Identifier: CA1479994790
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1721646151

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99421020_99421021insC , CM000666.2:g.99421020_99421021insC GRCh38
NC_000004.11:g.100342177_100342178insC , CM000666.1:g.100342177_100342178insC GRCh37
NC_000004.10:g.100561200_100561201insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-228_565-227insG MANE Select ENSP00000414254.2:n.565-228_565-227insG
ENST00000209665.8:c.601-228_601-227insG ENSP00000209665.4:n.601-228_601-227insG
ENST00000437033.6:c.565-228_565-227insG ENSP00000414254.2:n.565-228_565-227insG
ENST00000476959.5:c.625-228_625-227insG ENSP00000420269.1:n.625-228_625-227insG
ENST00000482593.5:c.394-228_394-227insG ENSP00000420613.1:n.394-228_394-227insG
NM_000673.4:c.601-228_601-227insG NP_000664.2:n.601-228_601-227insG
NM_001166504.1:c.625-228_625-227insG NP_001159976.1:n.625-228_625-227insG
NM_000673.7:c.565-228_565-227insG MANE Select NP_000664.3:n.565-228_565-227insG
NM_001166504.2:c.625-228_625-227insG NP_001159976.1:n.625-228_625-227insG