Canonical Allele Identifier: CA458881419

Gene: ASB10

Linked Data

• dbSNP Id: rs151344619
• gnomAD v2: 7-150883927-A-G
• gnomAD v4: 7-151186840-A-G
• MyVariant Identifiers: chr7:g.150883927A>G (hg19) ; chr7:g.151186840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186840A>G , CM000669.2:g.151186840A>G	GRCh38
NC_000007.13:g.150883927A>G , CM000669.1:g.150883927A>G	GRCh37
NC_000007.12:g.150514860A>G	NCBI36
NG_017016.1:g.5993T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.291T>C MANE Select	ENSP00000391137.2:p.Asp97=
ENST00000275838.5:c.291T>C	ENSP00000275838.1:p.Asp97=
ENST00000377867.7:c.272-181T>C	ENSP00000367098.3:n.272-181T>C
ENST00000415615.1:c.*335T>C	ENSP00000410871.1:n.*335T>C
ENST00000420175.2:c.291T>C	ENSP00000391137.2:p.Asp97=
NM_001142459.1:c.291T>C	NP_001135931.2:p.Asp97=
NM_001142460.1:c.291T>C	NP_001135932.2:p.Asp97=
NM_080871.3:c.272-181T>C	NP_543147.2:n.272-181T>C
XM_005249949.3:c.426T>C	XP_005250006.1:p.Asp142=
NM_001142459.2:c.291T>C MANE Select	NP_001135931.2:p.Asp97=
NM_080871.4:c.272-181T>C	NP_543147.2:n.272-181T>C