Canonical Allele Identifier: CA2336597689

Gene: CEACAM5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41717515C= , CM000681.2:g.41717515C=	GRCh38
NC_000019.9:g.42221434C= , CM000681.1:g.42221434C=	GRCh37
NC_000019.8:g.46913274C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004363.6:c.1019C= MANE Select	NP_004354.3:p.Ala340=
ENST00000221992.11:c.1019C= MANE Select	ENSP00000221992.5:p.Ala340=
NM_001291484.1:c.1019C=	NP_001278413.1:p.Ala340=
NM_001291484.2:c.1019C=	NP_001278413.1:p.Ala340=
NM_001291484.3:c.1019C=	NP_001278413.1:p.Ala340=
NM_001308398.1:c.1016C=	NP_001295327.1:p.Ala339=
NM_001308398.2:c.1016C=	NP_001295327.1:p.Ala339=
NM_004363.4:c.1019C=	NP_004354.3:p.Ala340=
NM_004363.5:c.1019C=	NP_004354.3:p.Ala340=
ENST00000221992.10:c.1019C=	ENSP00000221992.5:p.Ala340=
ENST00000398599.8:c.1016C=	ENSP00000381600.4:p.Ala339=
ENST00000405816.5:c.1019C=	ENSP00000385072.1:p.Ala340=
ENST00000435837.2:c.64+8720C=	ENSP00000469926.1:n.64+8720C=
ENST00000595113.1:c.466C=
ENST00000595403.1:c.325-2415C=
ENST00000598976.1:c.424+7476C=	ENSP00000469421.1:n.424+7476C=
ENST00000615021.4:c.485C=	ENSP00000482157.1:p.Ala162=
ENST00000616453.1:c.612+2357C=	ENSP00000480800.1:n.612+2357C=
ENST00000617332.4:c.1019C=	ENSP00000482303.1:p.Ala340=
XM_005258413.3:c.1019C=	XP_005258470.2:p.Ala340=
XM_011526322.1:c.704-613C=	XP_011524624.1:n.704-613C=
XM_011526322.2:c.704-613C=	XP_011524624.1:n.704-613C=
XM_017026145.2:c.1016C=	XP_016881634.1:p.Ala339=
XM_017026146.2:c.764C=	XP_016881635.1:p.Ala255=