Canonical Allele Identifier: CA4573904

Gene: ASB10

Linked Data

• dbSNP Id: rs377623437
• ExAC: 7:150883687 G / A
• gnomAD v2: 7-150883687-G-A
• gnomAD v3: 7-151186600-G-A
• gnomAD v4: 7-151186600-G-A
• MyVariant Identifiers: chr7:g.150883687G>A (hg19) ; chr7:g.151186600G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186600G>A , CM000669.2:g.151186600G>A	GRCh38
NC_000007.13:g.150883687G>A , CM000669.1:g.150883687G>A	GRCh37
NC_000007.12:g.150514620G>A	NCBI36
NG_017016.1:g.6233C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.376C>T MANE Select	ENSP00000391137.2:p.Arg126Cys
ENST00000275838.5:c.376C>T	ENSP00000275838.1:p.Arg126Cys
ENST00000377867.7:c.331C>T	ENSP00000367098.3:p.Arg111Cys
ENST00000420175.2:c.376C>T	ENSP00000391137.2:p.Arg126Cys
NM_001142459.1:c.376C>T	NP_001135931.2:p.Arg126Cys
NM_001142460.1:c.376C>T	NP_001135932.2:p.Arg126Cys
NM_080871.3:c.331C>T	NP_543147.2:p.Arg111Cys
XM_005249949.3:c.511C>T	XP_005250006.1:p.Arg171Cys
NM_001142459.2:c.376C>T MANE Select	NP_001135931.2:p.Arg126Cys
NM_080871.4:c.331C>T	NP_543147.2:p.Arg111Cys