Canonical Allele Identifier: CA2303791227

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52752339C= , CM000680.2:g.52752339C=	GRCh38
NC_000018.9:g.50278709C= , CM000680.1:g.50278709C=	GRCh37
NC_000018.8:g.48532707C=	NCBI36
NG_013341.1:g.417168C=
NG_013341.2:g.417168C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.377C= MANE Select	NP_005206.2:p.Ser126=
ENST00000442544.7:c.377C= MANE Select	ENSP00000389140.2:p.Ser126=
NM_005215.3:c.377C=	NP_005206.2:p.Ser126=
ENST00000304775.12:c.178C=
ENST00000412726.5:c.308C=	ENSP00000397322.2:p.Ser103=
ENST00000442544.6:c.377C=	ENSP00000389140.2:p.Ser126=
ENST00000578080.1:c.280C=
ENST00000579349.1:c.174C=
ENST00000579666.1:n.166C=
ENST00000580024.1:n.181C=
ENST00000581559.1:c.173C=	ENSP00000463463.1:p.Ser58=
ENST00000582595.1:n.110C=
ENST00000582875.1:c.179C=	ENSP00000463131.1:p.Ser60=
XM_011525843.1:c.377C=	XP_011524145.1:p.Ser126=
XM_011525845.1:c.377C=	XP_011524147.1:p.Ser126=
XM_011525846.1:c.377C=	XP_011524148.1:p.Ser126=
XM_017025568.1:c.377C=	XP_016881057.1:p.Ser126=
XM_017025569.1:c.377C=	XP_016881058.1:p.Ser126=