Canonical Allele Identifier: CA458881492

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883523A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186436A>G , CM000669.2:g.151186436A>G	GRCh38
NC_000007.13:g.150883523A>G , CM000669.1:g.150883523A>G	GRCh37
NC_000007.12:g.150514456A>G	NCBI36
NG_017016.1:g.6397T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.540T>C MANE Select	ENSP00000391137.2:p.Asp180=
ENST00000275838.5:c.540T>C	ENSP00000275838.1:p.Asp180=
ENST00000377867.7:c.495T>C	ENSP00000367098.3:p.Asp165=
ENST00000420175.2:c.540T>C	ENSP00000391137.2:p.Asp180=
NM_001142459.1:c.540T>C	NP_001135931.2:p.Asp180=
NM_001142460.1:c.540T>C	NP_001135932.2:p.Asp180=
NM_080871.3:c.495T>C	NP_543147.2:p.Asp165=
XM_005249949.3:c.675T>C	XP_005250006.1:p.Asp225=
NM_001142459.2:c.540T>C MANE Select	NP_001135931.2:p.Asp180=
NM_080871.4:c.495T>C	NP_543147.2:p.Asp165=