Canonical Allele Identifier: CA7468851

Gene: CDIN1

Linked Data

• ClinVar Variation Id: 257533
• ClinVar RCV Id: RCV000252130 ; RCV001651153
• dbSNP Id: rs7183415
• ExAC: 15:36983962 T / C
• gnomAD v2: 15-36983962-T-C
• gnomAD v3: 15-36691761-T-C
• gnomAD v4: 15-36691761-T-C
• MyVariant Identifiers: chr15:g.36983962T>C (hg19) ; chr15:g.36691761T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36691761T>C , CM000677.2:g.36691761T>C	GRCh38
NC_000015.9:g.36983962T>C , CM000677.1:g.36983962T>C	GRCh37
NC_000015.8:g.34771254T>C	NCBI36
NG_034055.1:g.117159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000566621.6:c.423T>C MANE Select	ENSP00000455397.1:p.Tyr141=
ENST00000569302.6:c.423T>C	ENSP00000456477.1:p.Tyr141=
ENST00000570265.6:c.423T>C	ENSP00000493669.1:p.Tyr141=
ENST00000642817.1:c.*203T>C	ENSP00000495947.1:n.*203T>C
ENST00000643612.1:c.54T>C	ENSP00000496325.1:p.Tyr18=
ENST00000646533.1:c.423T>C	ENSP00000494718.1:p.Tyr141=
ENST00000646657.1:c.*55T>C	ENSP00000495542.1:n.*55T>C
ENST00000338183.8:c.129T>C	ENSP00000342433.4:p.Tyr43=
ENST00000437989.6:c.423T>C	ENSP00000401362.2:p.Tyr141=
ENST00000562877.5:c.129T>C	ENSP00000457854.1:p.Tyr43=
ENST00000566621.5:c.423T>C	ENSP00000455397.1:p.Tyr141=
ENST00000566807.5:c.129T>C	ENSP00000454831.1:p.Tyr43=
ENST00000567389.5:c.129T>C	ENSP00000456736.1:p.Tyr43=
ENST00000569302.5:c.423T>C	ENSP00000456477.1:p.Tyr141=
ENST00000570265.5:n.650T>C
NM_001130010.2:c.423T>C	NP_001123482.1:p.Tyr141=
NM_001290232.1:c.129T>C	NP_001277161.1:p.Tyr43=
NM_001290233.1:c.423T>C	NP_001277162.1:p.Tyr141=
NM_032499.5:c.129T>C	NP_115888.1:p.Tyr43=
XM_011522110.1:c.423T>C	XP_011520412.1:p.Tyr141=
XM_011522111.1:c.423T>C	XP_011520413.1:p.Tyr141=
XM_011522112.1:c.129T>C	XP_011520414.1:p.Tyr43=
XR_931921.1:n.673T>C
XR_931922.1:n.673T>C
XR_931923.1:n.673T>C
XR_931924.1:n.673T>C
NM_001321756.1:c.129T>C	NP_001308685.1:p.Tyr43=
NM_001321757.1:c.54T>C	NP_001308686.1:p.Tyr18=
NM_001321758.1:c.312T>C	NP_001308687.1:p.Tyr104=
NM_001321759.1:c.423T>C	NP_001308688.1:p.Tyr141=
NM_001321760.1:c.423T>C	NP_001308689.1:p.Tyr141=
NM_001321761.1:c.423T>C	NP_001308690.1:p.Tyr141=
XM_017022676.1:c.347-17462T>C	XP_016878165.1:n.347-17462T>C
XM_017022677.1:c.347-17462T>C	XP_016878166.1:n.347-17462T>C
XM_024450088.1:c.129T>C	XP_024305856.1:p.Tyr43=
XR_002957689.1:n.597-17462T>C
NM_001321759.2:c.423T>C MANE Select	NP_001308688.1:p.Tyr141=
NM_001130010.3:c.423T>C	NP_001123482.1:p.Tyr141=
NM_001290232.2:c.129T>C	NP_001277161.1:p.Tyr43=
NM_001290233.2:c.423T>C	NP_001277162.1:p.Tyr141=
NM_001321756.2:c.129T>C	NP_001308685.1:p.Tyr43=
NM_001321757.2:c.54T>C	NP_001308686.1:p.Tyr18=
NM_001321758.2:c.312T>C	NP_001308687.1:p.Tyr104=
NM_001321760.2:c.423T>C	NP_001308689.1:p.Tyr141=
NM_001321761.2:c.423T>C	NP_001308690.1:p.Tyr141=
NM_032499.6:c.129T>C	NP_115888.1:p.Tyr43=