Canonical Allele Identifier: CA458881589

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883625A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186538A>G , CM000669.2:g.151186538A>G	GRCh38
NC_000007.13:g.150883625A>G , CM000669.1:g.150883625A>G	GRCh37
NC_000007.12:g.150514558A>G	NCBI36
NG_017016.1:g.6295T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.438T>C MANE Select	ENSP00000391137.2:p.Pro146=
ENST00000275838.5:c.438T>C	ENSP00000275838.1:p.Pro146=
ENST00000377867.7:c.393T>C	ENSP00000367098.3:p.Pro131=
ENST00000420175.2:c.438T>C	ENSP00000391137.2:p.Pro146=
NM_001142459.1:c.438T>C	NP_001135931.2:p.Pro146=
NM_001142460.1:c.438T>C	NP_001135932.2:p.Pro146=
NM_080871.3:c.393T>C	NP_543147.2:p.Pro131=
XM_005249949.3:c.573T>C	XP_005250006.1:p.Pro191=
NM_001142459.2:c.438T>C MANE Select	NP_001135931.2:p.Pro146=
NM_080871.4:c.393T>C	NP_543147.2:p.Pro131=