Canonical Allele Identifier: CA1479841147

Gene: ADH5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99078405_99078409delinsCAGAA , CM000666.2:g.99078405_99078409delinsCAGAA	GRCh38
NC_000004.11:g.99999556_99999560delinsCAGAA , CM000666.1:g.99999556_99999560delinsCAGAA	GRCh37
NC_000004.10:g.100218579_100218583delinsCAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296412.14:c.345-1486_345-1482delinsTTCTG MANE Select	ENSP00000296412.8:n.345-1486_345-1482delinsTTCTG
ENST00000296412.13:c.345-1486_345-1482delinsTTCTG	ENSP00000296412.8:n.345-1486_345-1482delinsTTCTG
ENST00000296412.12:c.345-1486_345-1482delinsTTCTG	ENSP00000296412.8:n.345-1486_345-1482delinsTTCTG
ENST00000502590.5:c.*25-1486_*25-1482delinsTTCTG	ENSP00000422119.1:n.*25-1486_*25-1482delinsTTCTG
ENST00000503130.5:c.306-1486_306-1482delinsTTCTG	ENSP00000427049.1:n.306-1486_306-1482delinsTTCTG
ENST00000505652.1:c.*168+1411_*168+1415delinsTTCTG	ENSP00000421556.1:n.*168+1411_*168+1415delinsTTCTG
ENST00000508511.5:n.362-1486_362-1482delinsTTCTG
ENST00000512604.1:n.204+1411_204+1415delinsTTCTG
ENST00000512621.5:n.333-1486_333-1482delinsTTCTG
ENST00000512659.5:c.*32-1486_*32-1482delinsTTCTG	ENSP00000424650.1:n.*32-1486_*32-1482delinsTTCTG
ENST00000512991.5:n.543-1486_543-1482delinsTTCTG
ENST00000626055.2:c.*32-1486_*32-1482delinsTTCTG	ENSP00000487496.1:n.*32-1486_*32-1482delinsTTCTG
NM_000671.4:c.345-1486_345-1482delinsTTCTG MANE Select	NP_000662.3:n.345-1486_345-1482delinsTTCTG