Canonical Allele Identifier: CA780414457

Gene: DCC

Linked Data

• dbSNP Id: rs1311776181
• MyVariant Identifiers: chr18:g.50906091_50906092insT (hg19) ; chr18:g.53379721_53379722insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53379725dup , CM000680.2:g.53379725dup	GRCh38
NC_000018.9:g.50906095dup , CM000680.1:g.50906095dup	GRCh37
NC_000018.8:g.49160093dup	NCBI36
NG_013341.1:g.1044554dup
NG_013341.2:g.1044554dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2360-6318dup MANE Select	ENSP00000389140.2:n.2360-6318dup
ENST00000304775.12:c.2161-6318dup
ENST00000412726.5:c.2291-6318dup	ENSP00000397322.2:n.2291-6318dup
ENST00000442544.6:c.2360-6318dup	ENSP00000389140.2:n.2360-6318dup
ENST00000581580.5:c.1325-6318dup	ENSP00000464582.1:n.1325-6318dup
NM_005215.3:c.2360-6318dup	NP_005206.2:n.2360-6318dup
XM_011525843.1:c.2360-6318dup	XP_011524145.1:n.2360-6318dup
XM_011525844.1:c.1325-6318dup	XP_011524146.1:n.1325-6318dup
XM_011525845.1:c.2360-6318dup	XP_011524147.1:n.2360-6318dup
XM_011525846.1:c.2360-6318dup	XP_011524148.1:n.2360-6318dup
XM_011525844.2:c.1325-6318dup	XP_011524146.1:n.1325-6318dup
XM_017025568.1:c.2360-6318dup	XP_016881057.1:n.2360-6318dup
XM_017025569.1:c.2360-6318dup	XP_016881058.1:n.2360-6318dup
XM_017025570.1:c.1325-6318dup	XP_016881059.1:n.1325-6318dup
NM_005215.4:c.2360-6318dup MANE Select	NP_005206.2:n.2360-6318dup