Canonical Allele Identifier: CA370035922

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883560A>G (hg19) ; chr7:g.151186473A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186473A>G , CM000669.2:g.151186473A>G	GRCh38
NC_000007.13:g.150883560A>G , CM000669.1:g.150883560A>G	GRCh37
NC_000007.12:g.150514493A>G	NCBI36
NG_017016.1:g.6360T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.503T>C MANE Select	ENSP00000391137.2:p.Leu168Pro
ENST00000275838.5:c.503T>C	ENSP00000275838.1:p.Leu168Pro
ENST00000377867.7:c.458T>C	ENSP00000367098.3:p.Leu153Pro
ENST00000420175.2:c.503T>C	ENSP00000391137.2:p.Leu168Pro
NM_001142459.1:c.503T>C	NP_001135931.2:p.Leu168Pro
NM_001142460.1:c.503T>C	NP_001135932.2:p.Leu168Pro
NM_080871.3:c.458T>C	NP_543147.2:p.Leu153Pro
XM_005249949.3:c.638T>C	XP_005250006.1:p.Leu213Pro
NM_001142459.2:c.503T>C MANE Select	NP_001135931.2:p.Leu168Pro
NM_080871.4:c.458T>C	NP_543147.2:p.Leu153Pro