Canonical Allele Identifier: CA9503163

Gene: CEACAM16 CEACAM16-AS1

Linked Data

• ClinVar Variation Id: 281644
• ClinVar RCV Id: RCV000313285 ; RCV004021084
• dbSNP Id: rs61729706
• ExAC: 19:45209067 C / T
• gnomAD v2: 19-45209067-C-T
• gnomAD v3: 19-44705797-C-T
• gnomAD v4: 19-44705797-C-T
• MyVariant Identifiers: chr19:g.45209067C>T (hg19) ; chr19:g.44705797C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44705797C>T , CM000681.2:g.44705797C>T	GRCh38
NC_000019.9:g.45209067C>T , CM000681.1:g.45209067C>T	GRCh37
NC_000019.8:g.49900907C>T	NCBI36
NG_032692.2:g.11647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587331.7:c.869C>T (CEACAM16) MANE Select	ENSP00000466561.1:p.Thr290Met
ENST00000405314.2:c.869C>T (CEACAM16)	ENSP00000385576.1:p.Thr290Met
ENST00000587331.5:c.869C>T (CEACAM16)	ENSP00000466561.1:p.Thr290Met
NM_001039213.3:c.869C>T (CEACAM16)	NP_001034302.2:p.Thr290Met
XM_011526951.1:c.869C>T (CEACAM16)	XP_011525253.1:p.Thr290Met
NM_001039213.4:c.869C>T (CEACAM16) MANE Select	NP_001034302.2:p.Thr290Met
XM_017026795.1:c.869C>T (CEACAM16)	XP_016882284.1:p.Thr290Met
XR_001753953.1:n.436-6620G>A (CEACAM16-AS1)
XR_001753954.1:n.373-6620G>A (CEACAM16-AS1)