Canonical Allele Identifier: CA1338125902

Gene: ASB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238440835C= , CM000664.2:g.238440835C=	GRCh38
NC_000002.11:g.239349476C= , CM000664.1:g.239349476C=	GRCh37
NC_000002.10:g.239014215C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264607.9:c.495-3507C= MANE Select	ENSP00000264607.4:n.495-3507C=
ENST00000264607.8:c.495-3507C=	ENSP00000264607.4:n.495-3507C=
ENST00000409297.1:c.192-3507C=	ENSP00000387025.1:n.192-3507C=
ENST00000438264.5:c.*167-3507C=	ENSP00000411773.1:n.*167-3507C=
ENST00000463352.5:n.536-3507C=
ENST00000468122.1:n.94-3507C=
ENST00000491653.1:n.686-3507C=
NM_001040445.1:c.495-3507C=	NP_001035535.1:n.495-3507C=
XM_005246080.1:c.192-3507C=	XP_005246137.1:n.192-3507C=
XR_241236.1:n.825-3507C=
XR_241237.1:n.825-3507C=
NM_001040445.2:c.495-3507C=	NP_001035535.1:n.495-3507C=
NM_001330196.1:c.192-3507C=	NP_001317125.1:n.192-3507C=
NM_001040445.3:c.495-3507C= MANE Select	NP_001035535.1:n.495-3507C=
NM_001330196.2:c.192-3507C=	NP_001317125.1:n.192-3507C=