Canonical Allele Identifier: CA2641856368

Gene: DCC

Linked Data

• gnomAD v4: 18-53207956-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53207956_53207957insT , CM000680.2:g.53207956_53207957insT	GRCh38
NC_000018.9:g.50734326_50734327insT , CM000680.1:g.50734326_50734327insT	GRCh37
NC_000018.8:g.48988324_48988325insT	NCBI36
NG_013341.1:g.872785_872786insT
NG_013341.2:g.872785_872786insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.1861+139_1861+140insT MANE Select	ENSP00000389140.2:n.1861+139_1861+140insT
ENST00000304775.12:c.1662+139_1662+140insT
ENST00000412726.5:c.1792+139_1792+140insT	ENSP00000397322.2:n.1792+139_1792+140insT
ENST00000442544.6:c.1861+139_1861+140insT	ENSP00000389140.2:n.1861+139_1861+140insT
ENST00000581580.5:c.826+139_826+140insT	ENSP00000464582.1:n.826+139_826+140insT
NM_005215.3:c.1861+139_1861+140insT	NP_005206.2:n.1861+139_1861+140insT
XM_011525843.1:c.1861+139_1861+140insT	XP_011524145.1:n.1861+139_1861+140insT
XM_011525844.1:c.826+139_826+140insT	XP_011524146.1:n.826+139_826+140insT
XM_011525845.1:c.1861+139_1861+140insT	XP_011524147.1:n.1861+139_1861+140insT
XM_011525846.1:c.1861+139_1861+140insT	XP_011524148.1:n.1861+139_1861+140insT
XM_011525844.2:c.826+139_826+140insT	XP_011524146.1:n.826+139_826+140insT
XM_017025568.1:c.1861+139_1861+140insT	XP_016881057.1:n.1861+139_1861+140insT
XM_017025569.1:c.1861+139_1861+140insT	XP_016881058.1:n.1861+139_1861+140insT
XM_017025570.1:c.826+139_826+140insT	XP_016881059.1:n.826+139_826+140insT
NM_005215.4:c.1861+139_1861+140insT MANE Select	NP_005206.2:n.1861+139_1861+140insT