Canonical Allele Identifier: CA458881478

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883972A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186885A>C , CM000669.2:g.151186885A>C	GRCh38
NC_000007.13:g.150883972A>C , CM000669.1:g.150883972A>C	GRCh37
NC_000007.12:g.150514905A>C	NCBI36
NG_017016.1:g.5948T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.246T>G MANE Select	ENSP00000391137.2:p.Ala82=
ENST00000275838.5:c.246T>G	ENSP00000275838.1:p.Ala82=
ENST00000377867.7:c.272-226T>G	ENSP00000367098.3:n.272-226T>G
ENST00000415615.1:c.*290T>G	ENSP00000410871.1:n.*290T>G
ENST00000420175.2:c.246T>G	ENSP00000391137.2:p.Ala82=
NM_001142459.1:c.246T>G	NP_001135931.2:p.Ala82=
NM_001142460.1:c.246T>G	NP_001135932.2:p.Ala82=
NM_080871.3:c.272-226T>G	NP_543147.2:n.272-226T>G
XM_005249949.3:c.381T>G	XP_005250006.1:p.Ala127=
NM_001142459.2:c.246T>G MANE Select	NP_001135931.2:p.Ala82=
NM_080871.4:c.272-226T>G	NP_543147.2:n.272-226T>G