Canonical Allele Identifier: CA370037567
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186932C>A , CM000669.2:g.151186932C>A GRCh38
NC_000007.13:g.150884019C>A , CM000669.1:g.150884019C>A GRCh37
NC_000007.12:g.150514952C>A NCBI36
NG_017016.1:g.5901G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.199G>T MANE Select ENSP00000391137.2:p.Val67Leu
ENST00000275838.5:c.199G>T ENSP00000275838.1:p.Val67Leu
ENST00000377867.7:c.272-273G>T ENSP00000367098.3:n.272-273G>T
ENST00000415615.1:c.*243G>T ENSP00000410871.1:n.*243G>T
ENST00000420175.2:c.199G>T ENSP00000391137.2:p.Val67Leu
NM_001142459.1:c.199G>T NP_001135931.2:p.Val67Leu
NM_001142460.1:c.199G>T NP_001135932.2:p.Val67Leu
NM_080871.3:c.272-273G>T NP_543147.2:n.272-273G>T
XM_005249949.3:c.334G>T XP_005250006.1:p.Val112Leu
NM_001142459.2:c.199G>T MANE Select NP_001135931.2:p.Val67Leu
NM_080871.4:c.272-273G>T NP_543147.2:n.272-273G>T