Canonical Allele Identifier: CA458881278

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883484G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186397G>C , CM000669.2:g.151186397G>C	GRCh38
NC_000007.13:g.150883484G>C , CM000669.1:g.150883484G>C	GRCh37
NC_000007.12:g.150514417G>C	NCBI36
NG_017016.1:g.6436C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.579C>G MANE Select	ENSP00000391137.2:p.Thr193=
ENST00000275838.5:c.579C>G	ENSP00000275838.1:p.Thr193=
ENST00000377867.7:c.534C>G	ENSP00000367098.3:p.Thr178=
ENST00000420175.2:c.579C>G	ENSP00000391137.2:p.Thr193=
NM_001142459.1:c.579C>G	NP_001135931.2:p.Thr193=
NM_001142460.1:c.579C>G	NP_001135932.2:p.Thr193=
NM_080871.3:c.534C>G	NP_543147.2:p.Thr178=
XM_005249949.3:c.714C>G	XP_005250006.1:p.Thr238=
NM_001142459.2:c.579C>G MANE Select	NP_001135931.2:p.Thr193=
NM_080871.4:c.534C>G	NP_543147.2:p.Thr178=