Canonical Allele Identifier: CA1479942164

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307817_99307818delinsCA , CM000666.2:g.99307817_99307818delinsCA	GRCh38
NC_000004.11:g.100228974_100228975delinsCA , CM000666.1:g.100228974_100228975delinsCA	GRCh37
NC_000004.10:g.100447997_100447998delinsCA	NCBI36
NG_011435.1:g.18598_18599delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*22_*23delinsTG MANE Select	ENSP00000306606.8:n.*22_*23delinsTG
ENST00000305046.12:c.*22_*23delinsTG	ENSP00000306606.8:n.*22_*23delinsTG
ENST00000506651.5:c.*22_*23delinsTG	ENSP00000425998.2:n.*22_*23delinsTG
ENST00000515694.4:n.3245_3246delinsTG
ENST00000625860.2:c.*22_*23delinsTG	ENSP00000486614.1:n.*22_*23delinsTG
NM_000668.5:c.*22_*23delinsTG	NP_000659.2:n.*22_*23delinsTG
NM_001286650.1:c.*22_*23delinsTG	NP_001273579.1:n.*22_*23delinsTG
NM_000668.6:c.*22_*23delinsTG MANE Select	NP_000659.2:n.*22_*23delinsTG
NM_001286650.2:c.*22_*23delinsTG	NP_001273579.1:n.*22_*23delinsTG