Canonical Allele Identifier: CA2576506471

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906163_52906165del , CM000680.2:g.52906163_52906165del	GRCh38
NC_000018.9:g.50432533_50432535del , CM000680.1:g.50432533_50432535del	GRCh37
NC_000018.8:g.48686531_48686533del	NCBI36
NG_013341.1:g.570992_570994del
NG_013341.2:g.570992_570994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.532_534del MANE Select	ENSP00000389140.2:p.Gln178del
ENST00000304775.12:c.333_335del
ENST00000412726.5:c.463_465del	ENSP00000397322.2:p.Gln155del
ENST00000442544.6:c.532_534del	ENSP00000389140.2:p.Gln178del
ENST00000579349.1:c.453_455del
ENST00000580024.1:n.445_447del
ENST00000581559.1:c.453_455del	ENSP00000463463.1:n.453_455del
NM_005215.3:c.532_534del	NP_005206.2:p.Gln178del
XM_011525843.1:c.532_534del	XP_011524145.1:p.Gln178del
XM_011525845.1:c.532_534del	XP_011524147.1:p.Gln178del
XM_011525846.1:c.532_534del	XP_011524148.1:p.Gln178del
XM_017025568.1:c.532_534del	XP_016881057.1:p.Gln178del
XM_017025569.1:c.532_534del	XP_016881058.1:p.Gln178del
NM_005215.4:c.532_534del MANE Select	NP_005206.2:p.Gln178del