Canonical Allele Identifier: CA380827741

Gene: INCENP

Linked Data

• dbSNP Id: rs1675126
• gnomAD v4: 11-62138902-T-G
• MyVariant Identifiers: chr11:g.61906374T>G (hg19) ; chr11:g.62138902T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62138902T>G , CM000673.2:g.62138902T>G	GRCh38
NC_000011.9:g.61906374T>G , CM000673.1:g.61906374T>G	GRCh37
NC_000011.8:g.61662950T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394818.8:c.1188T>G MANE Select	ENSP00000378295.3:p.Asn396Lys
ENST00000278849.4:c.1188T>G	ENSP00000278849.4:p.Asn396Lys
ENST00000394818.7:c.1188T>G	ENSP00000378295.3:p.Asn396Lys
ENST00000528375.1:n.157T>G
NM_001040694.1:c.1188T>G	NP_001035784.1:p.Asn396Lys
NM_020238.2:c.1188T>G	NP_064623.2:p.Asn396Lys
XM_006718533.1:c.1188T>G	XP_006718596.1:p.Asn396Lys
XM_011544995.1:c.1188T>G	XP_011543297.1:p.Asn396Lys
XM_011544996.1:c.1188T>G	XP_011543298.1:p.Asn396Lys
XM_011544997.1:c.1188T>G	XP_011543299.1:p.Asn396Lys
XM_011544998.1:c.1188T>G	XP_011543300.1:p.Asn396Lys
XM_006718533.3:c.1188T>G	XP_006718596.1:p.Asn396Lys
XM_011544995.3:c.1188T>G	XP_011543297.1:p.Asn396Lys
XM_011544996.3:c.1188T>G	XP_011543298.1:p.Asn396Lys
XM_011544997.2:c.1188T>G	XP_011543299.1:p.Asn396Lys
XM_011544998.3:c.1188T>G	XP_011543300.1:p.Asn396Lys
NM_001040694.2:c.1188T>G MANE Select	NP_001035784.1:p.Asn396Lys
NM_020238.3:c.1188T>G	NP_064623.2:p.Asn396Lys