Canonical Allele Identifier: CA536522
Community Standard Title: NM_003036.4(SKI):c.985C>T (p.Pro329Ser)
Gene: SKI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2302993C>T , CM000663.2:g.2302993C>T GRCh38
NC_000001.10:g.2234432C>T , CM000663.1:g.2234432C>T GRCh37
NC_000001.9:g.2224292C>T NCBI36
NG_013084.1:g.79299C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003036.4:c.985C>T MANE Select NP_003027.1:p.Pro329Ser
ENST00000378536.5:c.985C>T MANE Select ENSP00000367797.4:p.Pro329Ser
NM_003036.3:c.985C>T NP_003027.1:p.Pro329Ser
ENST00000378536.4:c.985C>T ENSP00000367797.4:p.Pro329Ser
ENST00000478223.2:n.92C>T
ENST00000508416.1:n.207C>T
ENST00000704337.1:n.153C>T
XM_005244775.2:c.985C>T XP_005244832.1:p.Pro329Ser
XM_005244775.3:c.985C>T XP_005244832.1:p.Pro329Ser
XM_005244776.3:c.115C>T XP_005244833.1:p.Pro39Ser
XM_005244776.4:c.115C>T XP_005244833.1:p.Pro39Ser
XM_017002128.1:c.493C>T XP_016857617.1:p.Pro165Ser