Canonical Allele Identifier: CA7468800

Gene: CDIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36657892C>T , CM000677.2:g.36657892C>T	GRCh38
NC_000015.9:g.36950093C>T , CM000677.1:g.36950093C>T	GRCh37
NC_000015.8:g.34737385C>T	NCBI36
NG_034055.1:g.83290C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001321759.2:c.333C>T MANE Select	NP_001308688.1:p.His111=
ENST00000566621.6:c.333C>T MANE Select	ENSP00000455397.1:p.His111=
NM_001130010.2:c.333C>T	NP_001123482.1:p.His111=
NM_001130010.3:c.333C>T	NP_001123482.1:p.His111=
NM_001290232.1:c.39C>T	NP_001277161.1:p.His13=
NM_001290232.2:c.39C>T	NP_001277161.1:p.His13=
NM_001290233.1:c.333C>T	NP_001277162.1:p.His111=
NM_001290233.2:c.333C>T	NP_001277162.1:p.His111=
NM_001321756.1:c.39C>T	NP_001308685.1:p.His13=
NM_001321756.2:c.39C>T	NP_001308685.1:p.His13=
NM_001321757.1:c.-71C>T	NP_001308686.1:n.-71C>T
NM_001321757.2:c.-71C>T	NP_001308686.1:n.-71C>T
NM_001321758.1:c.222C>T	NP_001308687.1:p.His74=
NM_001321758.2:c.222C>T	NP_001308687.1:p.His74=
NM_001321759.1:c.333C>T	NP_001308688.1:p.His111=
NM_001321760.1:c.333C>T	NP_001308689.1:p.His111=
NM_001321760.2:c.333C>T	NP_001308689.1:p.His111=
NM_001321761.1:c.333C>T	NP_001308690.1:p.His111=
NM_001321761.2:c.333C>T	NP_001308690.1:p.His111=
NM_032499.5:c.39C>T	NP_115888.1:p.His13=
NM_032499.6:c.39C>T	NP_115888.1:p.His13=
ENST00000338183.8:c.39C>T	ENSP00000342433.4:p.His13=
ENST00000437989.6:c.333C>T	ENSP00000401362.2:p.His111=
ENST00000562877.5:c.39C>T	ENSP00000457854.1:p.His13=
ENST00000564586.5:c.222C>T	ENSP00000457227.1:p.His74=
ENST00000566621.5:c.333C>T	ENSP00000455397.1:p.His111=
ENST00000566807.5:c.39C>T	ENSP00000454831.1:p.His13=
ENST00000567389.5:c.39C>T	ENSP00000456736.1:p.His13=
ENST00000569302.5:c.333C>T	ENSP00000456477.1:p.His111=
ENST00000569302.6:c.333C>T	ENSP00000456477.1:p.His111=
ENST00000570265.5:n.560C>T
ENST00000570265.6:c.333C>T	ENSP00000493669.1:p.His111=
ENST00000642817.1:c.*113C>T	ENSP00000495947.1:n.*113C>T
ENST00000643612.1:c.-146C>T	ENSP00000496325.1:n.-146C>T
ENST00000643837.1:n.507C>T
ENST00000646533.1:c.333C>T	ENSP00000494718.1:p.His111=
ENST00000646657.1:c.333C>T	ENSP00000495542.1:p.His111=
ENST00000647059.1:n.126C>T
XM_011522110.1:c.333C>T	XP_011520412.1:p.His111=
XM_011522111.1:c.333C>T	XP_011520413.1:p.His111=
XM_011522112.1:c.39C>T	XP_011520414.1:p.His13=
XM_017022676.1:c.333C>T	XP_016878165.1:p.His111=
XM_017022677.1:c.333C>T	XP_016878166.1:p.His111=
XM_024450088.1:c.39C>T	XP_024305856.1:p.His13=
XR_002957689.1:n.583C>T
XR_931921.1:n.583C>T
XR_931922.1:n.583C>T
XR_931923.1:n.583C>T
XR_931924.1:n.583C>T