Canonical Allele Identifier: CA2294676179

Gene: CCDC178

Linked Data

• dbSNP Id: rs6507016

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33347811C>G , CM000680.2:g.33347811C>G	GRCh38
NC_000018.9:g.30927775C>G , CM000680.1:g.30927775C>G	GRCh37
NC_000018.8:g.29181773C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000383096.8:c.457+1079G>C MANE Select	ENSP00000372576.3:n.457+1079G>C
ENST00000300227.12:c.457+1079G>C	ENSP00000300227.8:n.457+1079G>C
ENST00000383096.7:c.457+1079G>C	ENSP00000372576.3:n.457+1079G>C
ENST00000399177.7:c.457+1079G>C	ENSP00000382130.3:n.457+1079G>C
ENST00000403303.5:c.457+1079G>C	ENSP00000385591.1:n.457+1079G>C
ENST00000406524.6:c.457+1079G>C	ENSP00000385867.2:n.457+1079G>C
ENST00000579916.5:c.348+22239G>C	ENSP00000462153.1:n.348+22239G>C
ENST00000579947.5:c.457+1079G>C	ENSP00000462370.1:n.457+1079G>C
ENST00000583930.5:c.457+1079G>C	ENSP00000463254.1:n.457+1079G>C
NM_001105528.1:c.457+1079G>C	NP_001098998.1:n.457+1079G>C
NM_001308126.1:c.457+1079G>C	NP_001295055.1:n.457+1079G>C
NM_198995.2:c.457+1079G>C	NP_945346.2:n.457+1079G>C
XM_011525943.1:c.457+1079G>C	XP_011524245.1:n.457+1079G>C
XM_011525944.1:c.457+1079G>C	XP_011524246.1:n.457+1079G>C
XM_011525945.1:c.457+1079G>C	XP_011524247.1:n.457+1079G>C
XM_011525947.1:c.457+1079G>C	XP_011524249.1:n.457+1079G>C
XM_011525948.1:c.457+1079G>C	XP_011524250.1:n.457+1079G>C
XM_011525949.1:c.457+1079G>C	XP_011524251.1:n.457+1079G>C
XM_011525950.1:c.457+1079G>C	XP_011524252.1:n.457+1079G>C
XM_011525951.1:c.457+1079G>C	XP_011524253.1:n.457+1079G>C
XM_011525952.1:c.-30+1079G>C	XP_011524254.1:n.-30+1079G>C
XM_011525953.1:c.-30+1079G>C	XP_011524255.1:n.-30+1079G>C
XM_011525954.1:c.457+1079G>C	XP_011524256.1:n.457+1079G>C
XM_011525955.1:c.457+1079G>C	XP_011524257.1:n.457+1079G>C
XM_011525954.2:c.457+1079G>C	XP_011524256.1:n.457+1079G>C
XM_017025721.1:c.457+1079G>C	XP_016881210.1:n.457+1079G>C
XM_017025722.1:c.457+1079G>C	XP_016881211.1:n.457+1079G>C
XM_017025723.1:c.457+1079G>C	XP_016881212.1:n.457+1079G>C
XM_017025724.1:c.-30+1079G>C	XP_016881213.1:n.-30+1079G>C
XM_017025725.1:c.-30+1079G>C	XP_016881214.1:n.-30+1079G>C
NM_001105528.3:c.457+1079G>C	NP_001098998.1:n.457+1079G>C
NM_001308126.3:c.457+1079G>C	NP_001295055.1:n.457+1079G>C
NM_001371120.1:c.457+1079G>C	NP_001358049.1:n.457+1079G>C
NM_001371121.1:c.457+1079G>C	NP_001358050.1:n.457+1079G>C
NM_198995.3:c.457+1079G>C	NP_945346.2:n.457+1079G>C
NM_001105528.4:c.457+1079G>C MANE Select	NP_001098998.1:n.457+1079G>C