Canonical Allele Identifier: CA402473120

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53410572A>G , CM000680.2:g.53410572A>G	GRCh38
NC_000018.9:g.50936942A>G , CM000680.1:g.50936942A>G	GRCh37
NC_000018.8:g.49190940A>G	NCBI36
NG_013341.1:g.1075401A>G
NG_013341.2:g.1075401A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.3056A>G MANE Select	NP_005206.2:p.Tyr1019Cys
ENST00000442544.7:c.3056A>G MANE Select	ENSP00000389140.2:p.Tyr1019Cys
NM_005215.3:c.3056A>G	NP_005206.2:p.Tyr1019Cys
ENST00000304775.12:c.2624A>G
ENST00000412726.5:c.2987A>G	ENSP00000397322.2:p.Tyr996Cys
ENST00000442544.6:c.3056A>G	ENSP00000389140.2:p.Tyr1019Cys
ENST00000579941.1:c.472A>G
ENST00000581580.5:c.1961A>G	ENSP00000464582.1:p.Tyr654Cys
XM_011525843.1:c.3056A>G	XP_011524145.1:p.Tyr1019Cys
XM_011525844.1:c.2021A>G	XP_011524146.1:p.Tyr674Cys
XM_011525844.2:c.2021A>G	XP_011524146.1:p.Tyr674Cys
XM_011525845.1:c.3056A>G	XP_011524147.1:p.Tyr1019Cys
XM_011525846.1:c.2996A>G	XP_011524148.1:p.Tyr999Cys
XM_017025568.1:c.3056A>G	XP_016881057.1:p.Tyr1019Cys
XM_017025569.1:c.2996A>G	XP_016881058.1:p.Tyr999Cys
XM_017025570.1:c.2021A>G	XP_016881059.1:p.Tyr674Cys