Canonical Allele Identifier: CA536703
Community Standard Title: NM_003036.4(SKI):c.1411G>T (p.Val471Leu)
Gene: SKI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2304039G>T , CM000663.2:g.2304039G>T GRCh38
NC_000001.10:g.2235478G>T , CM000663.1:g.2235478G>T GRCh37
NC_000001.9:g.2225338G>T NCBI36
NG_013084.1:g.80345G>T

Transcript Alleles

HGVS Amino-acid Change
NM_003036.4:c.1411G>T MANE Select NP_003027.1:p.Val471Leu
ENST00000378536.5:c.1411G>T MANE Select ENSP00000367797.4:p.Val471Leu
NM_003036.3:c.1411G>T NP_003027.1:p.Val471Leu
ENST00000378536.4:c.1411G>T ENSP00000367797.4:p.Val471Leu
ENST00000507179.1:n.394G>T
XM_005244775.2:c.1411G>T XP_005244832.1:p.Val471Leu
XM_005244775.3:c.1411G>T XP_005244832.1:p.Val471Leu
XM_005244776.3:c.541G>T XP_005244833.1:p.Val181Leu
XM_005244776.4:c.541G>T XP_005244833.1:p.Val181Leu
XM_017002128.1:c.919G>T XP_016857617.1:p.Val307Leu