Canonical Allele Identifier: CA2641858837

Gene: DCC

Linked Data

• gnomAD v4: 18-53467875-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53467875A>T , CM000680.2:g.53467875A>T	GRCh38
NC_000018.9:g.50994245A>T , CM000680.1:g.50994245A>T	GRCh37
NC_000018.8:g.49248243A>T	NCBI36
NG_013341.1:g.1132704A>T
NG_013341.2:g.1132704A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.3620-19A>T MANE Select	ENSP00000389140.2:n.3620-19A>T
ENST00000412726.5:c.3551-19A>T	ENSP00000397322.2:n.3551-19A>T
ENST00000442544.6:c.3620-19A>T	ENSP00000389140.2:n.3620-19A>T
ENST00000581580.5:c.2525-19A>T	ENSP00000464582.1:n.2525-19A>T
NM_005215.3:c.3620-19A>T	NP_005206.2:n.3620-19A>T
XM_011525843.1:c.3620-19A>T	XP_011524145.1:n.3620-19A>T
XM_011525844.1:c.2585-19A>T	XP_011524146.1:n.2585-19A>T
XM_011525844.2:c.2585-19A>T	XP_011524146.1:n.2585-19A>T
XM_017025568.1:c.3620-19A>T	XP_016881057.1:n.3620-19A>T
XM_017025569.1:c.3560-19A>T	XP_016881058.1:n.3560-19A>T
XM_017025570.1:c.2585-19A>T	XP_016881059.1:n.2585-19A>T
NM_005215.4:c.3620-19A>T MANE Select	NP_005206.2:n.3620-19A>T