Canonical Allele Identifier: CA458881655

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883676C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186589C>G , CM000669.2:g.151186589C>G	GRCh38
NC_000007.13:g.150883676C>G , CM000669.1:g.150883676C>G	GRCh37
NC_000007.12:g.150514609C>G	NCBI36
NG_017016.1:g.6244G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.387G>C MANE Select	ENSP00000391137.2:p.Thr129=
ENST00000275838.5:c.387G>C	ENSP00000275838.1:p.Thr129=
ENST00000377867.7:c.342G>C	ENSP00000367098.3:p.Thr114=
ENST00000420175.2:c.387G>C	ENSP00000391137.2:p.Thr129=
NM_001142459.1:c.387G>C	NP_001135931.2:p.Thr129=
NM_001142460.1:c.387G>C	NP_001135932.2:p.Thr129=
NM_080871.3:c.342G>C	NP_543147.2:p.Thr114=
XM_005249949.3:c.522G>C	XP_005250006.1:p.Thr174=
NM_001142459.2:c.387G>C MANE Select	NP_001135931.2:p.Thr129=
NM_080871.4:c.342G>C	NP_543147.2:p.Thr114=