Canonical Allele Identifier: CA458881620

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884023C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186936C>G , CM000669.2:g.151186936C>G	GRCh38
NC_000007.13:g.150884023C>G , CM000669.1:g.150884023C>G	GRCh37
NC_000007.12:g.150514956C>G	NCBI36
NG_017016.1:g.5897G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.195G>C MANE Select	ENSP00000391137.2:p.Gly65=
ENST00000275838.5:c.195G>C	ENSP00000275838.1:p.Gly65=
ENST00000377867.7:c.272-277G>C	ENSP00000367098.3:n.272-277G>C
ENST00000415615.1:c.*239G>C	ENSP00000410871.1:n.*239G>C
ENST00000420175.2:c.195G>C	ENSP00000391137.2:p.Gly65=
NM_001142459.1:c.195G>C	NP_001135931.2:p.Gly65=
NM_001142460.1:c.195G>C	NP_001135932.2:p.Gly65=
NM_080871.3:c.272-277G>C	NP_543147.2:n.272-277G>C
XM_005249949.3:c.330G>C	XP_005250006.1:p.Gly110=
NM_001142459.2:c.195G>C MANE Select	NP_001135931.2:p.Gly65=
NM_080871.4:c.272-277G>C	NP_543147.2:n.272-277G>C