Canonical Allele Identifier: CA7468896

Gene: CDIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36692208T>C , CM000677.2:g.36692208T>C	GRCh38
NC_000015.9:g.36984409T>C , CM000677.1:g.36984409T>C	GRCh37
NC_000015.8:g.34771701T>C	NCBI36
NG_034055.1:g.117606T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000566621.6:c.476+33T>C MANE Select	ENSP00000455397.1:n.476+33T>C
ENST00000569302.6:c.476+33T>C	ENSP00000456477.1:n.476+33T>C
ENST00000570265.6:c.476+33T>C	ENSP00000493669.1:n.476+33T>C
ENST00000642817.1:c.*256+33T>C	ENSP00000495947.1:n.*256+33T>C
ENST00000643612.1:c.107+33T>C	ENSP00000496325.1:n.107+33T>C
ENST00000646533.1:c.476+33T>C	ENSP00000494718.1:n.476+33T>C
ENST00000646657.1:c.*108+33T>C	ENSP00000495542.1:n.*108+33T>C
ENST00000338183.8:c.182+33T>C	ENSP00000342433.4:n.182+33T>C
ENST00000437989.6:c.476+33T>C	ENSP00000401362.2:n.476+33T>C
ENST00000562877.5:c.182+33T>C	ENSP00000457854.1:n.182+33T>C
ENST00000566621.5:c.476+33T>C	ENSP00000455397.1:n.476+33T>C
ENST00000566807.5:c.182+33T>C	ENSP00000454831.1:n.182+33T>C
ENST00000567389.5:c.182+33T>C	ENSP00000456736.1:n.182+33T>C
ENST00000569302.5:c.476+33T>C	ENSP00000456477.1:n.476+33T>C
ENST00000570265.5:n.703+33T>C
NM_001130010.2:c.476+33T>C	NP_001123482.1:n.476+33T>C
NM_001290232.1:c.182+33T>C	NP_001277161.1:n.182+33T>C
NM_001290233.1:c.476+33T>C	NP_001277162.1:n.476+33T>C
NM_032499.5:c.182+33T>C	NP_115888.1:n.182+33T>C
XM_011522110.1:c.476+33T>C	XP_011520412.1:n.476+33T>C
XM_011522111.1:c.476+33T>C	XP_011520413.1:n.476+33T>C
XM_011522112.1:c.182+33T>C	XP_011520414.1:n.182+33T>C
XR_931921.1:n.726+33T>C
XR_931922.1:n.726+33T>C
XR_931923.1:n.726+33T>C
XR_931924.1:n.726+33T>C
NM_001321756.1:c.182+33T>C	NP_001308685.1:n.182+33T>C
NM_001321757.1:c.107+33T>C	NP_001308686.1:n.107+33T>C
NM_001321758.1:c.365+33T>C	NP_001308687.1:n.365+33T>C
NM_001321759.1:c.476+33T>C	NP_001308688.1:n.476+33T>C
NM_001321760.1:c.476+33T>C	NP_001308689.1:n.476+33T>C
NM_001321761.1:c.476+33T>C	NP_001308690.1:n.476+33T>C
XM_017022676.1:c.347-17015T>C	XP_016878165.1:n.347-17015T>C
XM_017022677.1:c.347-17015T>C	XP_016878166.1:n.347-17015T>C
XM_024450088.1:c.182+33T>C	XP_024305856.1:n.182+33T>C
XR_002957689.1:n.597-17015T>C
NM_001321759.2:c.476+33T>C MANE Select	NP_001308688.1:n.476+33T>C
NM_001130010.3:c.476+33T>C	NP_001123482.1:n.476+33T>C
NM_001290232.2:c.182+33T>C	NP_001277161.1:n.182+33T>C
NM_001290233.2:c.476+33T>C	NP_001277162.1:n.476+33T>C
NM_001321756.2:c.182+33T>C	NP_001308685.1:n.182+33T>C
NM_001321757.2:c.107+33T>C	NP_001308686.1:n.107+33T>C
NM_001321758.2:c.365+33T>C	NP_001308687.1:n.365+33T>C
NM_001321760.2:c.476+33T>C	NP_001308689.1:n.476+33T>C
NM_001321761.2:c.476+33T>C	NP_001308690.1:n.476+33T>C
NM_032499.6:c.182+33T>C	NP_115888.1:n.182+33T>C