Canonical Allele Identifier: CA9503130
Gene: CEACAM16 HGNC NCBI
CEACAM16-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 236048
dbSNP Id: rs746164064

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44705631C>T , CM000681.2:g.44705631C>T GRCh38
NC_000019.9:g.45208901C>T , CM000681.1:g.45208901C>T GRCh37
NC_000019.8:g.49900741C>T NCBI36
NG_032692.2:g.11481C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587331.7:c.703C>T (CEACAM16) MANE Select ENSP00000466561.1:p.Arg235Cys
ENST00000405314.2:c.703C>T (CEACAM16) ENSP00000385576.1:p.Arg235Cys
ENST00000587331.5:c.703C>T (CEACAM16) ENSP00000466561.1:p.Arg235Cys
NM_001039213.3:c.703C>T (CEACAM16) NP_001034302.2:p.Arg235Cys
XM_011526951.1:c.703C>T (CEACAM16) XP_011525253.1:p.Arg235Cys
NM_001039213.4:c.703C>T (CEACAM16) MANE Select NP_001034302.2:p.Arg235Cys
XM_017026795.1:c.703C>T (CEACAM16) XP_016882284.1:p.Arg235Cys
XR_001753953.1:n.436-6454G>A (CEACAM16-AS1)
XR_001753954.1:n.373-6454G>A (CEACAM16-AS1)