Canonical Allele Identifier: CA370037151

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186833-A-T
• MyVariant Identifiers: chr7:g.150883920A>T (hg19) ; chr7:g.151186833A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186833A>T , CM000669.2:g.151186833A>T	GRCh38
NC_000007.13:g.150883920A>T , CM000669.1:g.150883920A>T	GRCh37
NC_000007.12:g.150514853A>T	NCBI36
NG_017016.1:g.6000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.298T>A MANE Select	ENSP00000391137.2:p.Phe100Ile
ENST00000275838.5:c.298T>A	ENSP00000275838.1:p.Phe100Ile
ENST00000377867.7:c.272-174T>A	ENSP00000367098.3:n.272-174T>A
ENST00000415615.1:c.*342T>A	ENSP00000410871.1:n.*342T>A
ENST00000420175.2:c.298T>A	ENSP00000391137.2:p.Phe100Ile
NM_001142459.1:c.298T>A	NP_001135931.2:p.Phe100Ile
NM_001142460.1:c.298T>A	NP_001135932.2:p.Phe100Ile
NM_080871.3:c.272-174T>A	NP_543147.2:n.272-174T>A
XM_005249949.3:c.433T>A	XP_005250006.1:p.Phe145Ile
NM_001142459.2:c.298T>A MANE Select	NP_001135931.2:p.Phe100Ile
NM_080871.4:c.272-174T>A	NP_543147.2:n.272-174T>A