Canonical Allele Identifier: CA2838552710

Gene: CCDC186

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.114168802G>A , CM000672.2:g.114168802G>A	GRCh38
NC_000010.10:g.115928561G>A , CM000672.1:g.115928561G>A	GRCh37
NC_000010.9:g.115918551G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369287.8:c.-62+5213C>T MANE Select	ENSP00000358293.3:n.-62+5213C>T
ENST00000648613.1:c.-62+4339C>T	ENSP00000498136.1:n.-62+4339C>T
ENST00000369285.7:c.-62+4339C>T	ENSP00000358291.3:n.-62+4339C>T
ENST00000369286.1:c.-62+5213C>T	ENSP00000358292.1:n.-62+5213C>T
ENST00000369287.7:c.-62+5213C>T	ENSP00000358293.3:n.-62+5213C>T
NM_018017.2:c.-62+5213C>T	NP_060487.2:n.-62+5213C>T
XM_005269937.1:c.-62+4339C>T	XP_005269994.1:n.-62+4339C>T
XM_011539915.1:c.-110+5213C>T	XP_011538217.1:n.-110+5213C>T
NM_001321829.1:c.-62+4339C>T	NP_001308758.1:n.-62+4339C>T
NM_018017.3:c.-62+5213C>T	NP_060487.2:n.-62+5213C>T
NM_153249.1:c.-62+4339C>T	NP_694981.1:n.-62+4339C>T
NR_135815.1:n.331+4339C>T
XM_011539915.3:c.-110+5213C>T	XP_011538217.1:n.-110+5213C>T
XM_011539916.3:c.-62+5213C>T	XP_011538218.1:n.-62+5213C>T
NM_018017.4:c.-62+5213C>T MANE Select	NP_060487.2:n.-62+5213C>T