Canonical Allele Identifier: CA2303875008
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52906062_52906066delinsCACAG , CM000680.2:g.52906062_52906066delinsCACAG GRCh38
NC_000018.9:g.50432432_50432436delinsCACAG , CM000680.1:g.50432432_50432436delinsCACAG GRCh37
NC_000018.8:g.48686430_48686434delinsCACAG NCBI36
NG_013341.1:g.570891_570895delinsCACAG
NG_013341.2:g.570891_570895delinsCACAG

Transcript Alleles

HGVS Amino-acid change
ENST00000442544.7:c.431_435delinsCACAG MANE Select ENSP00000389140.2:p.Ser144=
ENST00000304775.12:c.232_236delinsCACAG
ENST00000412726.5:c.362_366delinsCACAG ENSP00000397322.2:p.Ser121=
ENST00000442544.6:c.431_435delinsCACAG ENSP00000389140.2:p.Ser144=
ENST00000579349.1:c.352_356delinsCACAG
ENST00000580024.1:n.344_348delinsCACAG
ENST00000581559.1:c.352_356delinsCACAG ENSP00000463463.1:n.352_356delinsCACAG
NM_005215.3:c.431_435delinsCACAG NP_005206.2:p.Ser144=
XM_011525843.1:c.431_435delinsCACAG XP_011524145.1:p.Ser144=
XM_011525845.1:c.431_435delinsCACAG XP_011524147.1:p.Ser144=
XM_011525846.1:c.431_435delinsCACAG XP_011524148.1:p.Ser144=
XM_017025568.1:c.431_435delinsCACAG XP_016881057.1:p.Ser144=
XM_017025569.1:c.431_435delinsCACAG XP_016881058.1:p.Ser144=
NM_005215.4:c.431_435delinsCACAG MANE Select NP_005206.2:p.Ser144=