Canonical Allele Identifier: CA503999334

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50432493T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906123T>C , CM000680.2:g.52906123T>C	GRCh38
NC_000018.9:g.50432493T>C , CM000680.1:g.50432493T>C	GRCh37
NC_000018.8:g.48686491T>C	NCBI36
NG_013341.1:g.570952T>C
NG_013341.2:g.570952T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.492T>C MANE Select	ENSP00000389140.2:p.Ile164=
ENST00000304775.12:c.293T>C
ENST00000412726.5:c.423T>C	ENSP00000397322.2:p.Ile141=
ENST00000442544.6:c.492T>C	ENSP00000389140.2:p.Ile164=
ENST00000579349.1:c.413T>C
ENST00000580024.1:n.405T>C
ENST00000581559.1:c.413T>C	ENSP00000463463.1:n.413T>C
NM_005215.3:c.492T>C	NP_005206.2:p.Ile164=
XM_011525843.1:c.492T>C	XP_011524145.1:p.Ile164=
XM_011525845.1:c.492T>C	XP_011524147.1:p.Ile164=
XM_011525846.1:c.492T>C	XP_011524148.1:p.Ile164=
XM_017025568.1:c.492T>C	XP_016881057.1:p.Ile164=
XM_017025569.1:c.492T>C	XP_016881058.1:p.Ile164=
NM_005215.4:c.492T>C MANE Select	NP_005206.2:p.Ile164=