Canonical Allele Identifier: CA406288237
Community Standard Title: NM_001039213.4(CEACAM16):c.459C>A (p.Cys153Ter)
Gene: CEACAM16 HGNC NCBI
CEACAM16-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44704094C>A , CM000681.2:g.44704094C>A GRCh38
NC_000019.9:g.45207364C>A , CM000681.1:g.45207364C>A GRCh37
NC_000019.8:g.49899204C>A NCBI36
NG_032692.2:g.9944C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001039213.4:c.459C>A (CEACAM16) MANE Select NP_001034302.2:p.Cys153Ter
ENST00000587331.7:c.459C>A (CEACAM16) MANE Select ENSP00000466561.1:p.Cys153Ter
NM_001039213.3:c.459C>A (CEACAM16) NP_001034302.2:p.Cys153Ter
ENST00000405314.2:c.459C>A (CEACAM16) ENSP00000385576.1:p.Cys153Ter
ENST00000587331.5:c.459C>A (CEACAM16) ENSP00000466561.1:p.Cys153Ter
XM_011526951.1:c.459C>A (CEACAM16) XP_011525253.1:p.Cys153Ter
XM_017026795.1:c.459C>A (CEACAM16) XP_016882284.1:p.Cys153Ter
XR_001753953.1:n.436-4917G>T (CEACAM16-AS1)
XR_001753954.1:n.373-4917G>T (CEACAM16-AS1)