Canonical Allele Identifier: CA406018613

Gene: CEACAM3

Linked Data

• MyVariant Identifiers: chr19:g.42301687T>G (hg19) ; chr19:g.41797755T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41797755T>G , CM000681.2:g.41797755T>G	GRCh38
NC_000019.9:g.42301687T>G , CM000681.1:g.42301687T>G	GRCh37
NC_000019.8:g.46993527T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357396.8:c.231T>G MANE Select	ENSP00000349971.3:p.Ser77Arg
ENST00000344550.4:c.231T>G	ENSP00000341725.4:p.Ser77Arg
ENST00000357396.7:c.231T>G	ENSP00000349971.3:p.Ser77Arg
ENST00000415495.5:c.231T>G	ENSP00000411641.1:p.Ser77Arg
ENST00000595255.1:n.319T>G
ENST00000596544.1:c.111T>G	ENSP00000469333.1:p.Ser37Arg
ENST00000599305.1:n.307T>G
ENST00000630848.2:c.231T>G	ENSP00000485920.1:p.Ser77Arg
NM_001277163.2:c.231T>G	NP_001264092.1:p.Ser77Arg
NM_001815.4:c.231T>G	NP_001806.2:p.Ser77Arg
NR_102333.2:n.319T>G
NM_001815.5:c.231T>G MANE Select	NP_001806.2:p.Ser77Arg
NM_001277163.3:c.231T>G	NP_001264092.1:p.Ser77Arg
NR_102333.3:n.322T>G