Canonical Allele Identifier: CA4573862

Gene: ASB10

Linked Data

• dbSNP Id: rs751734262
• ExAC: 7:150883544 G / T
• gnomAD v2: 7-150883544-G-T
• gnomAD v3: 7-151186457-G-T
• gnomAD v4: 7-151186457-G-T
• MyVariant Identifiers: chr7:g.150883544G>T (hg19) ; chr7:g.151186457G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186457G>T , CM000669.2:g.151186457G>T	GRCh38
NC_000007.13:g.150883544G>T , CM000669.1:g.150883544G>T	GRCh37
NC_000007.12:g.150514477G>T	NCBI36
NG_017016.1:g.6376C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.519C>A MANE Select	ENSP00000391137.2:p.Asp173Glu
ENST00000275838.5:c.519C>A	ENSP00000275838.1:p.Asp173Glu
ENST00000377867.7:c.474C>A	ENSP00000367098.3:p.Asp158Glu
ENST00000420175.2:c.519C>A	ENSP00000391137.2:p.Asp173Glu
NM_001142459.1:c.519C>A	NP_001135931.2:p.Asp173Glu
NM_001142460.1:c.519C>A	NP_001135932.2:p.Asp173Glu
NM_080871.3:c.474C>A	NP_543147.2:p.Asp158Glu
XM_005249949.3:c.654C>A	XP_005250006.1:p.Asp218Glu
NM_001142459.2:c.519C>A MANE Select	NP_001135931.2:p.Asp173Glu
NM_080871.4:c.474C>A	NP_543147.2:p.Asp158Glu