Canonical Allele Identifier: CA536657
Community Standard Title: NM_003036.4(SKI):c.1274C>T (p.Ala425Val)
Gene: SKI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2303902C>T , CM000663.2:g.2303902C>T GRCh38
NC_000001.10:g.2235341C>T , CM000663.1:g.2235341C>T GRCh37
NC_000001.9:g.2225201C>T NCBI36
NG_013084.1:g.80208C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003036.4:c.1274C>T MANE Select NP_003027.1:p.Ala425Val
ENST00000378536.5:c.1274C>T MANE Select ENSP00000367797.4:p.Ala425Val
NM_003036.3:c.1274C>T NP_003027.1:p.Ala425Val
ENST00000378536.4:c.1274C>T ENSP00000367797.4:p.Ala425Val
ENST00000507179.1:n.257C>T
ENST00000704337.1:n.442C>T
XM_005244775.2:c.1274C>T XP_005244832.1:p.Ala425Val
XM_005244775.3:c.1274C>T XP_005244832.1:p.Ala425Val
XM_005244776.3:c.404C>T XP_005244833.1:p.Ala135Val
XM_005244776.4:c.404C>T XP_005244833.1:p.Ala135Val
XM_017002128.1:c.782C>T XP_016857617.1:p.Ala261Val