Canonical Allele Identifier: CA406288437

Gene: CEACAM16 CEACAM16-AS1

Linked Data

• dbSNP Id: rs1325120027
• gnomAD v2: 19-45207411-G-A
• gnomAD v4: 19-44704141-G-A
• MyVariant Identifiers: chr19:g.45207411G>A (hg19) ; chr19:g.44704141G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44704141G>A , CM000681.2:g.44704141G>A	GRCh38
NC_000019.9:g.45207411G>A , CM000681.1:g.45207411G>A	GRCh37
NC_000019.8:g.49899251G>A	NCBI36
NG_032692.2:g.9991G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000587331.7:c.506G>A (CEACAM16) MANE Select	ENSP00000466561.1:p.Gly169Glu
ENST00000405314.2:c.506G>A (CEACAM16)	ENSP00000385576.1:p.Gly169Glu
ENST00000587331.5:c.506G>A (CEACAM16)	ENSP00000466561.1:p.Gly169Glu
NM_001039213.3:c.506G>A (CEACAM16)	NP_001034302.2:p.Gly169Glu
XM_011526951.1:c.506G>A (CEACAM16)	XP_011525253.1:p.Gly169Glu
NM_001039213.4:c.506G>A (CEACAM16) MANE Select	NP_001034302.2:p.Gly169Glu
XM_017026795.1:c.506G>A (CEACAM16)	XP_016882284.1:p.Gly169Glu
XR_001753953.1:n.436-4964C>T (CEACAM16-AS1)
XR_001753954.1:n.373-4964C>T (CEACAM16-AS1)