Canonical Allele Identifier: CA2838474554

Gene: CCNY

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.35347734T>G , CM000672.2:g.35347734T>G	GRCh38
NC_000010.10:g.35636662T>G , CM000672.1:g.35636662T>G	GRCh37
NC_000010.9:g.35676668T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374704.8:c.154+10527T>G MANE Select	ENSP00000363836.4:n.154+10527T>G
ENST00000265375.13:c.-72+10527T>G	ENSP00000265375.9:n.-72+10527T>G
ENST00000339497.7:c.154+10527T>G	ENSP00000344275.5:n.154+10527T>G
ENST00000374704.7:c.154+10527T>G	ENSP00000363836.4:n.154+10527T>G
ENST00000374706.5:c.-9+97108T>G	ENSP00000363838.1:n.-9+97108T>G
ENST00000490012.6:c.-116+15297T>G	ENSP00000473487.1:n.-116+15297T>G
ENST00000492478.5:n.156+10527T>G
ENST00000493157.6:c.-223-86379T>G	ENSP00000473625.1:n.-223-86379T>G
NM_001282852.1:c.154+10527T>G	NP_001269781.1:n.154+10527T>G
NM_001282853.1:c.-72+10527T>G	NP_001269782.1:n.-72+10527T>G
NM_001282854.1:c.-109+10527T>G	NP_001269783.1:n.-109+10527T>G
NM_145012.5:c.154+10527T>G	NP_659449.3:n.154+10527T>G
NM_181698.3:c.-9+97108T>G	NP_859049.2:n.-9+97108T>G
XM_005252388.1:c.13+240T>G	XP_005252445.1:n.13+240T>G
XM_011519357.1:c.154+10527T>G	XP_011517659.1:n.154+10527T>G
XM_011519358.1:c.-116+97108T>G	XP_011517660.1:n.-116+97108T>G
XM_011519359.1:c.-116+15297T>G	XP_011517661.1:n.-116+15297T>G
XM_011519360.1:c.-223-86379T>G	XP_011517662.1:n.-223-86379T>G
XM_011519361.1:c.-71-47082T>G	XP_011517663.1:n.-71-47082T>G
XM_011519362.1:c.-9+58303T>G	XP_011517664.1:n.-9+58303T>G
XM_011519363.1:c.-9+15297T>G	XP_011517665.1:n.-9+15297T>G
XM_011519364.1:c.-9+15297T>G	XP_011517666.1:n.-9+15297T>G
XM_011519365.1:c.-9+15297T>G	XP_011517667.1:n.-9+15297T>G
XM_011519366.1:c.-65-70180T>G	XP_011517668.1:n.-65-70180T>G
XM_011519369.1:c.-163+10527T>G	XP_011517671.1:n.-163+10527T>G
NM_145012.6:c.154+10527T>G MANE Select	NP_659449.3:n.154+10527T>G
NM_001282854.2:c.-109+10527T>G	NP_001269783.1:n.-109+10527T>G
NM_181698.4:c.-9+97108T>G	NP_859049.2:n.-9+97108T>G
NM_001282852.2:c.154+10527T>G	NP_001269781.1:n.154+10527T>G
NM_001282853.2:c.-72+10527T>G	NP_001269782.1:n.-72+10527T>G