Canonical Allele Identifier: CA11531961

Gene: ABHD6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58246932G>A , CM000665.2:g.58246932G>A	GRCh38
NC_000003.11:g.58232659G>A , CM000665.1:g.58232659G>A	GRCh37
NC_000003.10:g.58207699G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478253.6:c.-90-2946G>A MANE Select	ENSP00000420315.1:n.-90-2946G>A
ENST00000295962.8:c.-26+9016G>A	ENSP00000295962.4:n.-26+9016G>A
ENST00000463756.5:c.-90-2946G>A	ENSP00000420408.1:n.-90-2946G>A
ENST00000475982.5:c.-26+9016G>A	ENSP00000418209.1:n.-26+9016G>A
ENST00000478253.5:c.-90-2946G>A	ENSP00000420315.1:n.-90-2946G>A
ENST00000485900.1:c.-26+8288G>A	ENSP00000418934.1:n.-26+8288G>A
ENST00000613521.4:c.-26+9016G>A	ENSP00000484876.1:n.-26+9016G>A
NM_020676.5:c.-26+9016G>A	NP_065727.4:n.-26+9016G>A
XM_005265334.2:c.-90-2946G>A	XP_005265391.1:n.-90-2946G>A
XM_005265335.2:c.-26+9016G>A	XP_005265392.1:n.-26+9016G>A
XM_005265336.2:c.-90-2946G>A	XP_005265393.1:n.-90-2946G>A
NM_001320126.1:c.-90-2946G>A	NP_001307055.1:n.-90-2946G>A
NM_020676.6:c.-26+9016G>A	NP_065727.4:n.-26+9016G>A
XM_005265334.4:c.-90-2946G>A	XP_005265391.1:n.-90-2946G>A
XM_005265335.3:c.-26+9016G>A	XP_005265392.1:n.-26+9016G>A
NM_001320126.2:c.-90-2946G>A MANE Select	NP_001307055.1:n.-90-2946G>A
NM_020676.7:c.-26+9016G>A	NP_065727.4:n.-26+9016G>A