Canonical Allele Identifier: CA129787
Gene: CEACAM16 HGNC NCBI
CEACAM16-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 31238
ClinVar RCV Id: RCV000024237
dbSNP Id: rs387907149
MyVariant Identifiers: chr19:g.45207323A>C (hg19) chr19:g.44704053A>C (hg38)
PubMed: PMID:7655461 PMID:21368133
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44704053A>C , CM000681.2:g.44704053A>C GRCh38
NC_000019.9:g.45207323A>C , CM000681.1:g.45207323A>C GRCh37
NC_000019.8:g.49899163A>C NCBI36
NG_032692.2:g.9903A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000587331.7:c.418A>C (CEACAM16) MANE Select ENSP00000466561.1:p.Thr140Pro
ENST00000405314.2:c.418A>C (CEACAM16) ENSP00000385576.1:p.Thr140Pro
ENST00000587331.5:c.418A>C (CEACAM16) ENSP00000466561.1:p.Thr140Pro
NM_001039213.3:c.418A>C (CEACAM16) NP_001034302.2:p.Thr140Pro
XM_011526951.1:c.418A>C (CEACAM16) XP_011525253.1:p.Thr140Pro
NM_001039213.4:c.418A>C (CEACAM16) MANE Select NP_001034302.2:p.Thr140Pro
XM_017026795.1:c.418A>C (CEACAM16) XP_016882284.1:p.Thr140Pro
XR_001753953.1:n.436-4876T>G (CEACAM16-AS1)
XR_001753954.1:n.373-4876T>G (CEACAM16-AS1)
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