Canonical Allele Identifier: CA402513468

Gene: DCC

Linked Data

• gnomAD v4: 18-52906046-C-T
• COSMIC: COSM5904469
• MyVariant Identifiers: chr18:g.50432416C>T (hg19) ; chr18:g.52906046C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906046C>T , CM000680.2:g.52906046C>T	GRCh38
NC_000018.9:g.50432416C>T , CM000680.1:g.50432416C>T	GRCh37
NC_000018.8:g.48686414C>T	NCBI36
NG_013341.1:g.570875C>T
NG_013341.2:g.570875C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.415C>T MANE Select	ENSP00000389140.2:p.Pro139Ser
ENST00000304775.12:c.216C>T
ENST00000412726.5:c.346C>T	ENSP00000397322.2:p.Pro116Ser
ENST00000442544.6:c.415C>T	ENSP00000389140.2:p.Pro139Ser
ENST00000579349.1:c.336C>T
ENST00000580024.1:n.328C>T
ENST00000581559.1:c.336C>T	ENSP00000463463.1:n.336C>T
NM_005215.3:c.415C>T	NP_005206.2:p.Pro139Ser
XM_011525843.1:c.415C>T	XP_011524145.1:p.Pro139Ser
XM_011525845.1:c.415C>T	XP_011524147.1:p.Pro139Ser
XM_011525846.1:c.415C>T	XP_011524148.1:p.Pro139Ser
XM_017025568.1:c.415C>T	XP_016881057.1:p.Pro139Ser
XM_017025569.1:c.415C>T	XP_016881058.1:p.Pro139Ser
NM_005215.4:c.415C>T MANE Select	NP_005206.2:p.Pro139Ser