Canonical Allele Identifier: CA347156

Gene: DCC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.377C>A MANE Select	ENSP00000389140.2:p.Ser126Ter
ENST00000304775.12:c.178C>A
ENST00000412726.5:c.308C>A	ENSP00000397322.2:p.Ser103Ter
ENST00000442544.6:c.377C>A	ENSP00000389140.2:p.Ser126Ter
ENST00000578080.1:c.280C>A
ENST00000579349.1:c.174C>A
ENST00000579666.1:n.166C>A
ENST00000580024.1:n.181C>A
ENST00000581559.1:c.173C>A	ENSP00000463463.1:p.Ser58Ter
ENST00000582595.1:n.110C>A
ENST00000582875.1:c.179C>A	ENSP00000463131.1:p.Ser60Ter
NM_005215.3:c.377C>A	NP_005206.2:p.Ser126Ter
XM_011525843.1:c.377C>A	XP_011524145.1:p.Ser126Ter
XM_011525845.1:c.377C>A	XP_011524147.1:p.Ser126Ter
XM_011525846.1:c.377C>A	XP_011524148.1:p.Ser126Ter
XM_017025568.1:c.377C>A	XP_016881057.1:p.Ser126Ter
XM_017025569.1:c.377C>A	XP_016881058.1:p.Ser126Ter
NM_005215.4:c.377C>A MANE Select	NP_005206.2:p.Ser126Ter