Canonical Allele Identifier: CA2338067549
Gene: CEACAM16 HGNC NCBI
CEACAM16-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44704042T= , CM000681.2:g.44704042T= GRCh38
NC_000019.9:g.45207312T= , CM000681.1:g.45207312T= GRCh37
NC_000019.8:g.49899152T= NCBI36
NG_032692.2:g.9892T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587331.7:c.407T= (CEACAM16) MANE Select ENSP00000466561.1:p.Leu136=
ENST00000405314.2:c.407T= (CEACAM16) ENSP00000385576.1:p.Leu136=
ENST00000587331.5:c.407T= (CEACAM16) ENSP00000466561.1:p.Leu136=
NM_001039213.3:c.407T= (CEACAM16) NP_001034302.2:p.Leu136=
XM_011526951.1:c.407T= (CEACAM16) XP_011525253.1:p.Leu136=
NM_001039213.4:c.407T= (CEACAM16) MANE Select NP_001034302.2:p.Leu136=
XM_017026795.1:c.407T= (CEACAM16) XP_016882284.1:p.Leu136=
XR_001753953.1:n.436-4865A= (CEACAM16-AS1)
XR_001753954.1:n.373-4865A= (CEACAM16-AS1)