Canonical Allele Identifier: CA648883273

Gene: ADH1B

Linked Data

• COSMIC: COSN15448396

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307796_99307797insT , CM000666.2:g.99307796_99307797insT	GRCh38
NC_000004.11:g.100228953_100228954insT , CM000666.1:g.100228953_100228954insT	GRCh37
NC_000004.10:g.100447976_100447977insT	NCBI36
NG_011435.1:g.18619_18620insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.*43_*44insA MANE Select	ENSP00000306606.8:n.*43_*44insA
ENST00000305046.12:c.*43_*44insA	ENSP00000306606.8:n.*43_*44insA
ENST00000506651.5:c.*43_*44insA	ENSP00000425998.2:n.*43_*44insA
ENST00000515694.4:n.3266_3267insA
ENST00000625860.2:c.*43_*44insA	ENSP00000486614.1:n.*43_*44insA
NM_000668.5:c.*43_*44insA	NP_000659.2:n.*43_*44insA
NM_001286650.1:c.*43_*44insA	NP_001273579.1:n.*43_*44insA
NM_000668.6:c.*43_*44insA MANE Select	NP_000659.2:n.*43_*44insA
NM_001286650.2:c.*43_*44insA	NP_001273579.1:n.*43_*44insA