Canonical Allele Identifier: CA406288393

Gene: CEACAM16 CEACAM16-AS1

Linked Data

• MyVariant Identifiers: chr19:g.45207401T>C (hg19) ; chr19:g.44704131T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44704131T>C , CM000681.2:g.44704131T>C	GRCh38
NC_000019.9:g.45207401T>C , CM000681.1:g.45207401T>C	GRCh37
NC_000019.8:g.49899241T>C	NCBI36
NG_032692.2:g.9981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587331.7:c.496T>C (CEACAM16) MANE Select	ENSP00000466561.1:p.Phe166Leu
ENST00000405314.2:c.496T>C (CEACAM16)	ENSP00000385576.1:p.Phe166Leu
ENST00000587331.5:c.496T>C (CEACAM16)	ENSP00000466561.1:p.Phe166Leu
NM_001039213.3:c.496T>C (CEACAM16)	NP_001034302.2:p.Phe166Leu
XM_011526951.1:c.496T>C (CEACAM16)	XP_011525253.1:p.Phe166Leu
NM_001039213.4:c.496T>C (CEACAM16) MANE Select	NP_001034302.2:p.Phe166Leu
XM_017026795.1:c.496T>C (CEACAM16)	XP_016882284.1:p.Phe166Leu
XR_001753953.1:n.436-4954A>G (CEACAM16-AS1)
XR_001753954.1:n.373-4954A>G (CEACAM16-AS1)