Canonical Allele Identifier: CA15688059
Gene: INCENP HGNC NCBI

Linked Data

dbSNP Id: rs1047739

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62152221C>T , CM000673.2:g.62152221C>T GRCh38
NC_000011.9:g.61919693C>T , CM000673.1:g.61919693C>T GRCh37
NC_000011.8:g.61676269C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394818.8:c.*245C>T MANE Select ENSP00000378295.3:n.*245C>T
ENST00000278849.4:c.*245C>T ENSP00000278849.4:n.*245C>T
ENST00000394818.7:c.*245C>T ENSP00000378295.3:n.*245C>T
NM_001040694.1:c.*245C>T NP_001035784.1:n.*245C>T
NM_020238.2:c.*245C>T NP_064623.2:n.*245C>T
XM_006718533.1:c.*245C>T XP_006718596.1:n.*245C>T
XM_011544995.1:c.*245C>T XP_011543297.1:n.*245C>T
XM_011544996.1:c.*245C>T XP_011543298.1:n.*245C>T
XM_011544997.1:c.*245C>T XP_011543299.1:n.*245C>T
XM_011544998.1:c.*245C>T XP_011543300.1:n.*245C>T
XM_006718533.3:c.*245C>T XP_006718596.1:n.*245C>T
XM_011544995.3:c.*245C>T XP_011543297.1:n.*245C>T
XM_011544996.3:c.*245C>T XP_011543298.1:n.*245C>T
XM_011544997.2:c.*245C>T XP_011543299.1:n.*245C>T
XM_011544998.3:c.*245C>T XP_011543300.1:n.*245C>T
NM_001040694.2:c.*245C>T MANE Select NP_001035784.1:n.*245C>T
NM_020238.3:c.*245C>T NP_064623.2:n.*245C>T