Canonical Allele Identifier: CA14130030

Gene: CDIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36709632A>G , CM000677.2:g.36709632A>G	GRCh38
NC_000015.9:g.37001833A>G , CM000677.1:g.37001833A>G	GRCh37
NC_000015.8:g.34789125A>G	NCBI36
NG_034055.1:g.135030A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000566621.6:c.611-224A>G MANE Select	ENSP00000455397.1:n.611-224A>G
ENST00000569302.6:c.611-206A>G	ENSP00000456477.1:n.611-206A>G
ENST00000570265.6:c.611-224A>G	ENSP00000493669.1:n.611-224A>G
ENST00000642817.1:c.*391-224A>G	ENSP00000495947.1:n.*391-224A>G
ENST00000643612.1:c.242-224A>G	ENSP00000496325.1:n.242-224A>G
ENST00000646533.1:c.610+344A>G	ENSP00000494718.1:n.610+344A>G
ENST00000646657.1:c.*243-224A>G	ENSP00000495542.1:n.*243-224A>G
ENST00000338183.8:c.317-224A>G	ENSP00000342433.4:n.317-224A>G
ENST00000437989.6:c.611-224A>G	ENSP00000401362.2:n.611-224A>G
ENST00000562489.1:c.83-224A>G	ENSP00000454334.1:n.83-224A>G
ENST00000562877.5:c.317-224A>G	ENSP00000457854.1:n.317-224A>G
ENST00000565792.5:n.239-224A>G
ENST00000566621.5:c.611-224A>G	ENSP00000455397.1:n.611-224A>G
ENST00000566677.1:n.4977-224A>G
ENST00000566807.5:c.317-224A>G	ENSP00000454831.1:n.317-224A>G
ENST00000566932.5:n.142-224A>G
ENST00000567389.5:c.317-224A>G	ENSP00000456736.1:n.317-224A>G
ENST00000569302.5:c.611-206A>G	ENSP00000456477.1:n.611-206A>G
ENST00000570265.5:n.838-224A>G
NM_001130010.2:c.611-224A>G	NP_001123482.1:n.611-224A>G
NM_001290232.1:c.317-224A>G	NP_001277161.1:n.317-224A>G
NM_001290233.1:c.611-224A>G	NP_001277162.1:n.611-224A>G
NM_032499.5:c.317-224A>G	NP_115888.1:n.317-224A>G
XM_011522110.1:c.611-224A>G	XP_011520412.1:n.611-224A>G
XM_011522111.1:c.611-224A>G	XP_011520413.1:n.611-224A>G
XM_011522112.1:c.317-224A>G	XP_011520414.1:n.317-224A>G
XR_931921.1:n.861-224A>G
XR_931922.1:n.1718-224A>G
XR_931924.1:n.1692-224A>G
NM_001321756.1:c.317-224A>G	NP_001308685.1:n.317-224A>G
NM_001321757.1:c.242-224A>G	NP_001308686.1:n.242-224A>G
NM_001321758.1:c.500-224A>G	NP_001308687.1:n.500-224A>G
NM_001321759.1:c.611-224A>G	NP_001308688.1:n.611-224A>G
NM_001321760.1:c.610+344A>G	NP_001308689.1:n.610+344A>G
NM_001321761.1:c.611-206A>G	NP_001308690.1:n.611-206A>G
XM_017022676.1:c.413-224A>G	XP_016878165.1:n.413-224A>G
XM_017022677.1:c.413-224A>G	XP_016878166.1:n.413-224A>G
XM_024450088.1:c.317-224A>G	XP_024305856.1:n.317-224A>G
XR_002957689.1:n.663-224A>G
NM_001321759.2:c.611-224A>G MANE Select	NP_001308688.1:n.611-224A>G
NM_001130010.3:c.611-224A>G	NP_001123482.1:n.611-224A>G
NM_001290232.2:c.317-224A>G	NP_001277161.1:n.317-224A>G
NM_001290233.2:c.611-224A>G	NP_001277162.1:n.611-224A>G
NM_001321756.2:c.317-224A>G	NP_001308685.1:n.317-224A>G
NM_001321757.2:c.242-224A>G	NP_001308686.1:n.242-224A>G
NM_001321758.2:c.500-224A>G	NP_001308687.1:n.500-224A>G
NM_001321760.2:c.610+344A>G	NP_001308689.1:n.610+344A>G
NM_001321761.2:c.611-206A>G	NP_001308690.1:n.611-206A>G
NM_032499.6:c.317-224A>G	NP_115888.1:n.317-224A>G