Canonical Allele Identifier: CA14116510

Gene: CDIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36579756C>T , CM000677.2:g.36579756C>T	GRCh38
NC_000015.9:g.36871957C>T , CM000677.1:g.36871957C>T	GRCh37
NC_000015.8:g.34659249C>T	NCBI36
NG_034055.1:g.5154C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000566621.6:c.-105C>T MANE Select	ENSP00000455397.1:n.-105C>T
ENST00000569302.6:c.-105C>T	ENSP00000456477.1:n.-105C>T
ENST00000570265.6:c.-105C>T	ENSP00000493669.1:n.-105C>T
ENST00000642817.1:c.-105C>T	ENSP00000495947.1:n.-105C>T
ENST00000643837.1:n.70C>T
ENST00000646533.1:c.-105C>T	ENSP00000494718.1:n.-105C>T
ENST00000564586.5:c.-105C>T	ENSP00000457227.1:n.-105C>T
ENST00000566621.5:c.-105C>T	ENSP00000455397.1:n.-105C>T
ENST00000567573.5:n.119C>T
ENST00000570265.5:n.123C>T
NM_001130010.2:c.-105C>T	NP_001123482.1:n.-105C>T
NM_001290233.1:c.-105C>T	NP_001277162.1:n.-105C>T
XM_011522110.1:c.-105C>T	XP_011520412.1:n.-105C>T
XM_011522111.1:c.-105C>T	XP_011520413.1:n.-105C>T
XM_011522112.1:c.-353C>T	XP_011520414.1:n.-353C>T
XR_931921.1:n.146C>T
XR_931922.1:n.146C>T
XR_931923.1:n.146C>T
XR_931924.1:n.146C>T
NM_001321756.1:c.-353C>T	NP_001308685.1:n.-353C>T
NM_001321757.1:c.-508C>T	NP_001308686.1:n.-508C>T
NM_001321758.1:c.-105C>T	NP_001308687.1:n.-105C>T
NM_001321759.1:c.-105C>T	NP_001308688.1:n.-105C>T
NM_001321760.1:c.-105C>T	NP_001308689.1:n.-105C>T
NM_001321761.1:c.-105C>T	NP_001308690.1:n.-105C>T
XM_017022676.1:c.-105C>T	XP_016878165.1:n.-105C>T
XM_017022677.1:c.-105C>T	XP_016878166.1:n.-105C>T
XR_002957689.1:n.146C>T
NM_001321759.2:c.-105C>T MANE Select	NP_001308688.1:n.-105C>T
NM_001130010.3:c.-105C>T	NP_001123482.1:n.-105C>T
NM_001290233.2:c.-105C>T	NP_001277162.1:n.-105C>T
NM_001321756.2:c.-353C>T	NP_001308685.1:n.-353C>T
NM_001321757.2:c.-508C>T	NP_001308686.1:n.-508C>T
NM_001321758.2:c.-105C>T	NP_001308687.1:n.-105C>T
NM_001321760.2:c.-105C>T	NP_001308689.1:n.-105C>T
NM_001321761.2:c.-105C>T	NP_001308690.1:n.-105C>T