Canonical Allele Identifier: CA1338125854

Gene: ASB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238440712_238440716delinsTAGAG , CM000664.2:g.238440712_238440716delinsTAGAG	GRCh38
NC_000002.11:g.239349353_239349357delinsTAGAG , CM000664.1:g.239349353_239349357delinsTAGAG	GRCh37
NC_000002.10:g.239014092_239014096delinsTAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264607.9:c.495-3630_495-3626delinsTAGAG MANE Select	ENSP00000264607.4:n.495-3630_495-3626delinsTAGAG
ENST00000264607.8:c.495-3630_495-3626delinsTAGAG	ENSP00000264607.4:n.495-3630_495-3626delinsTAGAG
ENST00000409297.1:c.192-3630_192-3626delinsTAGAG	ENSP00000387025.1:n.192-3630_192-3626delinsTAGAG
ENST00000438264.5:c.*167-3630_*167-3626delinsTAGAG	ENSP00000411773.1:n.*167-3630_*167-3626delinsTAGAG
ENST00000463352.5:n.536-3630_536-3626delinsTAGAG
ENST00000468122.1:n.94-3630_94-3626delinsTAGAG
ENST00000491653.1:n.686-3630_686-3626delinsTAGAG
NM_001040445.1:c.495-3630_495-3626delinsTAGAG	NP_001035535.1:n.495-3630_495-3626delinsTAGAG
XM_005246080.1:c.192-3630_192-3626delinsTAGAG	XP_005246137.1:n.192-3630_192-3626delinsTAGAG
XR_241236.1:n.825-3630_825-3626delinsTAGAG
XR_241237.1:n.825-3630_825-3626delinsTAGAG
NM_001040445.2:c.495-3630_495-3626delinsTAGAG	NP_001035535.1:n.495-3630_495-3626delinsTAGAG
NM_001330196.1:c.192-3630_192-3626delinsTAGAG	NP_001317125.1:n.192-3630_192-3626delinsTAGAG
NM_001040445.3:c.495-3630_495-3626delinsTAGAG MANE Select	NP_001035535.1:n.495-3630_495-3626delinsTAGAG
NM_001330196.2:c.192-3630_192-3626delinsTAGAG	NP_001317125.1:n.192-3630_192-3626delinsTAGAG