Canonical Allele Identifier: CA503999344

Gene: DCC

Linked Data

• dbSNP Id: rs1292043584
• gnomAD v2: 18-50432508-A-C
• gnomAD v4: 18-52906138-A-C
• MyVariant Identifiers: chr18:g.50432508A>C (hg19) ; chr18:g.52906138A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906138A>C , CM000680.2:g.52906138A>C	GRCh38
NC_000018.9:g.50432508A>C , CM000680.1:g.50432508A>C	GRCh37
NC_000018.8:g.48686506A>C	NCBI36
NG_013341.1:g.570967A>C
NG_013341.2:g.570967A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.507A>C MANE Select	ENSP00000389140.2:p.Pro169=
ENST00000304775.12:c.308A>C
ENST00000412726.5:c.438A>C	ENSP00000397322.2:p.Pro146=
ENST00000442544.6:c.507A>C	ENSP00000389140.2:p.Pro169=
ENST00000579349.1:c.428A>C
ENST00000580024.1:n.420A>C
ENST00000581559.1:c.428A>C	ENSP00000463463.1:n.428A>C
NM_005215.3:c.507A>C	NP_005206.2:p.Pro169=
XM_011525843.1:c.507A>C	XP_011524145.1:p.Pro169=
XM_011525845.1:c.507A>C	XP_011524147.1:p.Pro169=
XM_011525846.1:c.507A>C	XP_011524148.1:p.Pro169=
XM_017025568.1:c.507A>C	XP_016881057.1:p.Pro169=
XM_017025569.1:c.507A>C	XP_016881058.1:p.Pro169=
NM_005215.4:c.507A>C MANE Select	NP_005206.2:p.Pro169=