Canonical Allele Identifier: CA1479942151

Gene: ADH1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307791_99307792delinsAG , CM000666.2:g.99307791_99307792delinsAG	GRCh38
NC_000004.11:g.100228948_100228949delinsAG , CM000666.1:g.100228948_100228949delinsAG	GRCh37
NC_000004.10:g.100447971_100447972delinsAG	NCBI36
NG_011435.1:g.18624_18625delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*48_*49delinsCT MANE Select	ENSP00000306606.8:n.*48_*49delinsCT
ENST00000305046.12:c.*48_*49delinsCT	ENSP00000306606.8:n.*48_*49delinsCT
ENST00000506651.5:c.*48_*49delinsCT	ENSP00000425998.2:n.*48_*49delinsCT
ENST00000515694.4:n.3271_3272delinsCT
ENST00000625860.2:c.*48_*49delinsCT	ENSP00000486614.1:n.*48_*49delinsCT
NM_000668.5:c.*48_*49delinsCT	NP_000659.2:n.*48_*49delinsCT
NM_001286650.1:c.*48_*49delinsCT	NP_001273579.1:n.*48_*49delinsCT
NM_000668.6:c.*48_*49delinsCT MANE Select	NP_000659.2:n.*48_*49delinsCT
NM_001286650.2:c.*48_*49delinsCT	NP_001273579.1:n.*48_*49delinsCT