Canonical Allele Identifier: CA308870149

Gene: CEACAM16 CEACAM16-AS1

Linked Data

• dbSNP Id: rs527797823
• gnomAD v3: 19-44704049-C-T
• gnomAD v4: 19-44704049-C-T
• MyVariant Identifiers: chr19:g.45207319C>T (hg19) ; chr19:g.44704049C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44704049C>T , CM000681.2:g.44704049C>T	GRCh38
NC_000019.9:g.45207319C>T , CM000681.1:g.45207319C>T	GRCh37
NC_000019.8:g.49899159C>T	NCBI36
NG_032692.2:g.9899C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587331.7:c.414C>T (CEACAM16) MANE Select	ENSP00000466561.1:p.Asn138=
ENST00000405314.2:c.414C>T (CEACAM16)	ENSP00000385576.1:p.Asn138=
ENST00000587331.5:c.414C>T (CEACAM16)	ENSP00000466561.1:p.Asn138=
NM_001039213.3:c.414C>T (CEACAM16)	NP_001034302.2:p.Asn138=
XM_011526951.1:c.414C>T (CEACAM16)	XP_011525253.1:p.Asn138=
NM_001039213.4:c.414C>T (CEACAM16) MANE Select	NP_001034302.2:p.Asn138=
XM_017026795.1:c.414C>T (CEACAM16)	XP_016882284.1:p.Asn138=
XR_001753953.1:n.436-4872G>A (CEACAM16-AS1)
XR_001753954.1:n.373-4872G>A (CEACAM16-AS1)