Canonical Allele Identifier: CA15688059
Gene: INCENP HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.62152221C>T
GRCh37 chr11:g.61919693C>T
gnomAD v2:
11:61919693 C / T
gnomAD v3:
11:62152221 C / T
gnomAD v4:
chr11-62152221-C-T
Joint Max Group AF 0.22727925 (NFE)
Genomes Max Group AF 0.23024303 (NFE)
Exomes Max Group AF 0.22582644 (NFE)
dbSNP:
1047739
JSON-LD

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
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