Canonical Allele Identifier: CA1140934989
Gene: SKI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2303352C= , CM000663.2:g.2303352C= GRCh38
NC_000001.10:g.2234791C= , CM000663.1:g.2234791C= GRCh37
NC_000001.9:g.2224651C= NCBI36
NG_013084.1:g.79658C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704337.1:n.331C=
ENST00000378536.5:c.1163C= MANE Select ENSP00000367797.4:p.Ala388=
ENST00000378536.4:c.1163C= ENSP00000367797.4:p.Ala388=
ENST00000478223.2:n.270C=
NM_003036.3:c.1163C= NP_003027.1:p.Ala388=
XM_005244775.2:c.1163C= XP_005244832.1:p.Ala388=
XM_005244776.3:c.293C= XP_005244833.1:p.Ala98=
XM_005244775.3:c.1163C= XP_005244832.1:p.Ala388=
XM_005244776.4:c.293C= XP_005244833.1:p.Ala98=
XM_017002128.1:c.671C= XP_016857617.1:p.Ala224=
NM_003036.4:c.1163C= MANE Select NP_003027.1:p.Ala388=