Canonical Allele Identifier: CA458881638

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186577-C-T
• MyVariant Identifiers: chr7:g.150883664C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186577C>T , CM000669.2:g.151186577C>T	GRCh38
NC_000007.13:g.150883664C>T , CM000669.1:g.150883664C>T	GRCh37
NC_000007.12:g.150514597C>T	NCBI36
NG_017016.1:g.6256G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.399G>A MANE Select	ENSP00000391137.2:p.Arg133=
ENST00000275838.5:c.399G>A	ENSP00000275838.1:p.Arg133=
ENST00000377867.7:c.354G>A	ENSP00000367098.3:p.Arg118=
ENST00000420175.2:c.399G>A	ENSP00000391137.2:p.Arg133=
NM_001142459.1:c.399G>A	NP_001135931.2:p.Arg133=
NM_001142460.1:c.399G>A	NP_001135932.2:p.Arg133=
NM_080871.3:c.354G>A	NP_543147.2:p.Arg118=
XM_005249949.3:c.534G>A	XP_005250006.1:p.Arg178=
NM_001142459.2:c.399G>A MANE Select	NP_001135931.2:p.Arg133=
NM_080871.4:c.354G>A	NP_543147.2:p.Arg118=