Canonical Allele Identifier: CA406288472
Gene: CEACAM16 HGNC NCBI
CEACAM16-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45207422G>T (hg19) chr19:g.44704152G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44704152G>T , CM000681.2:g.44704152G>T GRCh38
NC_000019.9:g.45207422G>T , CM000681.1:g.45207422G>T GRCh37
NC_000019.8:g.49899262G>T NCBI36
NG_032692.2:g.10002G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587331.7:c.517G>T (CEACAM16) MANE Select ENSP00000466561.1:p.Val173Phe
ENST00000405314.2:c.517G>T (CEACAM16) ENSP00000385576.1:p.Val173Phe
ENST00000587331.5:c.517G>T (CEACAM16) ENSP00000466561.1:p.Val173Phe
NM_001039213.3:c.517G>T (CEACAM16) NP_001034302.2:p.Val173Phe
XM_011526951.1:c.517G>T (CEACAM16) XP_011525253.1:p.Val173Phe
NM_001039213.4:c.517G>T (CEACAM16) MANE Select NP_001034302.2:p.Val173Phe
XM_017026795.1:c.517G>T (CEACAM16) XP_016882284.1:p.Val173Phe
XR_001753953.1:n.436-4975C>A (CEACAM16-AS1)
XR_001753954.1:n.373-4975C>A (CEACAM16-AS1)
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