Canonical Allele Identifier: CA1901645954

Gene: CCNY

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.35260329G>C , CM000672.2:g.35260329G>C	GRCh38
NC_000010.10:g.35549257G>C , CM000672.1:g.35549257G>C	GRCh37
NC_000010.9:g.35589263G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374706.5:c.-9+9703G>C	ENSP00000363838.1:n.-9+9703G>C
ENST00000490012.6:c.-325+9703G>C	ENSP00000473487.1:n.-325+9703G>C
ENST00000493157.6:c.-224+9703G>C	ENSP00000473625.1:n.-224+9703G>C
NM_181698.3:c.-9+9703G>C	NP_859049.2:n.-9+9703G>C
XM_011519358.1:c.-116+9703G>C	XP_011517660.1:n.-116+9703G>C
XM_011519359.1:c.-325+9703G>C	XP_011517661.1:n.-325+9703G>C
XM_011519360.1:c.-224+9703G>C	XP_011517662.1:n.-224+9703G>C
XM_011519361.1:c.-103+9703G>C	XP_011517663.1:n.-103+9703G>C
XM_011519362.1:c.-40+9703G>C	XP_011517664.1:n.-40+9703G>C
XM_011519363.1:c.-108+9703G>C	XP_011517665.1:n.-108+9703G>C
XM_011519364.1:c.-218+9703G>C	XP_011517666.1:n.-218+9703G>C
XM_011519365.1:c.-139+9703G>C	XP_011517667.1:n.-139+9703G>C
XM_011519366.1:c.-66+9703G>C	XP_011517668.1:n.-66+9703G>C
NM_181698.4:c.-9+9703G>C	NP_859049.2:n.-9+9703G>C