Canonical Allele Identifier: CA402518370

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53486808G>T , CM000680.2:g.53486808G>T	GRCh38
NC_000018.9:g.51013178G>T , CM000680.1:g.51013178G>T	GRCh37
NC_000018.8:g.49267176G>T	NCBI36
NG_013341.1:g.1151637G>T
NG_013341.2:g.1151637G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.3748G>T MANE Select	NP_005206.2:p.Ala1250Ser
ENST00000442544.7:c.3748G>T MANE Select	ENSP00000389140.2:p.Ala1250Ser
NM_005215.3:c.3748G>T	NP_005206.2:p.Ala1250Ser
ENST00000412726.5:c.3679G>T	ENSP00000397322.2:p.Ala1227Ser
ENST00000442544.6:c.3748G>T	ENSP00000389140.2:p.Ala1250Ser
ENST00000581580.5:c.2653G>T	ENSP00000464582.1:p.Ala885Ser
XM_011525843.1:c.3748G>T	XP_011524145.1:p.Ala1250Ser
XM_011525844.1:c.2713G>T	XP_011524146.1:p.Ala905Ser
XM_011525844.2:c.2713G>T	XP_011524146.1:p.Ala905Ser
XM_017025568.1:c.3748G>T	XP_016881057.1:p.Ala1250Ser
XM_017025569.1:c.3688G>T	XP_016881058.1:p.Ala1230Ser
XM_017025570.1:c.2713G>T	XP_016881059.1:p.Ala905Ser