Canonical Allele Identifier: CA370034655

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151181424C>T , CM000669.2:g.151181424C>T	GRCh38
NC_000007.13:g.150878511C>T , CM000669.1:g.150878511C>T	GRCh37
NC_000007.12:g.150509444C>T	NCBI36
NG_017016.1:g.11409G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001142459.2:c.619G>A MANE Select	NP_001135931.2:p.Val207Met
ENST00000420175.3:c.619G>A MANE Select	ENSP00000391137.2:p.Val207Met
NM_001142459.1:c.619G>A	NP_001135931.2:p.Val207Met
NM_001142460.1:c.619G>A	NP_001135932.2:p.Val207Met
NM_080871.3:c.574G>A	NP_543147.2:p.Val192Met
NM_080871.4:c.574G>A	NP_543147.2:p.Val192Met
ENST00000275838.5:c.619G>A	ENSP00000275838.1:p.Val207Met
ENST00000377867.7:c.574G>A	ENSP00000367098.3:p.Val192Met
ENST00000420175.2:c.619G>A	ENSP00000391137.2:p.Val207Met
XM_005249949.3:c.754G>A	XP_005250006.1:p.Val252Met