Canonical Allele Identifier: CA458881500

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883532A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186445A>C , CM000669.2:g.151186445A>C	GRCh38
NC_000007.13:g.150883532A>C , CM000669.1:g.150883532A>C	GRCh37
NC_000007.12:g.150514465A>C	NCBI36
NG_017016.1:g.6388T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.531T>G MANE Select	ENSP00000391137.2:p.Ala177=
ENST00000275838.5:c.531T>G	ENSP00000275838.1:p.Ala177=
ENST00000377867.7:c.486T>G	ENSP00000367098.3:p.Ala162=
ENST00000420175.2:c.531T>G	ENSP00000391137.2:p.Ala177=
NM_001142459.1:c.531T>G	NP_001135931.2:p.Ala177=
NM_001142460.1:c.531T>G	NP_001135932.2:p.Ala177=
NM_080871.3:c.486T>G	NP_543147.2:p.Ala162=
XM_005249949.3:c.666T>G	XP_005250006.1:p.Ala222=
NM_001142459.2:c.531T>G MANE Select	NP_001135931.2:p.Ala177=
NM_080871.4:c.486T>G	NP_543147.2:p.Ala162=