Canonical Allele Identifier: CA1479994727
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420964_99420967delinsAAGG , CM000666.2:g.99420964_99420967delinsAAGG GRCh38
NC_000004.11:g.100342121_100342124delinsAAGG , CM000666.1:g.100342121_100342124delinsAAGG GRCh37
NC_000004.10:g.100561144_100561147delinsAAGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-174_565-171delinsCCTT MANE Select ENSP00000414254.2:n.565-174_565-171delinsCCTT
ENST00000209665.8:c.601-174_601-171delinsCCTT ENSP00000209665.4:n.601-174_601-171delinsCCTT
ENST00000437033.6:c.565-174_565-171delinsCCTT ENSP00000414254.2:n.565-174_565-171delinsCCTT
ENST00000476959.5:c.625-174_625-171delinsCCTT ENSP00000420269.1:n.625-174_625-171delinsCCTT
ENST00000482593.5:c.394-174_394-171delinsCCTT ENSP00000420613.1:n.394-174_394-171delinsCCTT
NM_000673.4:c.601-174_601-171delinsCCTT NP_000664.2:n.601-174_601-171delinsCCTT
NM_001166504.1:c.625-174_625-171delinsCCTT NP_001159976.1:n.625-174_625-171delinsCCTT
NM_000673.7:c.565-174_565-171delinsCCTT MANE Select NP_000664.3:n.565-174_565-171delinsCCTT
NM_001166504.2:c.625-174_625-171delinsCCTT NP_001159976.1:n.625-174_625-171delinsCCTT