Canonical Allele Identifier: CA2576506469

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906048_52906049del , CM000680.2:g.52906048_52906049del	GRCh38
NC_000018.9:g.50432418_50432419del , CM000680.1:g.50432418_50432419del	GRCh37
NC_000018.8:g.48686416_48686417del	NCBI36
NG_013341.1:g.570877_570878del
NG_013341.2:g.570877_570878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.417_418del MANE Select	ENSP00000389140.2:p.Leu140GlufsTer22
ENST00000304775.12:c.218_219del
ENST00000412726.5:c.348_349del	ENSP00000397322.2:p.Leu117GlufsTer22
ENST00000442544.6:c.417_418del	ENSP00000389140.2:p.Leu140GlufsTer22
ENST00000579349.1:c.338_339del
ENST00000580024.1:n.330_331del
ENST00000581559.1:c.338_339del	ENSP00000463463.1:n.338_339del
NM_005215.3:c.417_418del	NP_005206.2:p.Leu140GlufsTer22
XM_011525843.1:c.417_418del	XP_011524145.1:p.Leu140GlufsTer22
XM_011525845.1:c.417_418del	XP_011524147.1:p.Leu140GlufsTer22
XM_011525846.1:c.417_418del	XP_011524148.1:p.Leu140GlufsTer22
XM_017025568.1:c.417_418del	XP_016881057.1:p.Leu140GlufsTer22
XM_017025569.1:c.417_418del	XP_016881058.1:p.Leu140GlufsTer22
NM_005215.4:c.417_418del MANE Select	NP_005206.2:p.Leu140GlufsTer22