Canonical Allele Identifier: CA16603398
Gene: KCND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 383943
ClinVar RCV Id: RCV000430266 RCV000757925 RCV002255097 RCV003223405
dbSNP Id: rs1057521793
MyVariant Identifiers: chr1:g.112329724C>T (hg19) chr1:g.111787102C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111787102C>T , CM000663.2:g.111787102C>T GRCh38
NC_000001.10:g.112329724C>T , CM000663.1:g.112329724C>T GRCh37
NC_000001.9:g.112131247C>T NCBI36
NG_032011.2:g.207054G>A , LRG_445:g.207054G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302127.5:c.1111G>A MANE Select ENSP00000306923.4:p.Gly371Arg
ENST00000302127.4:c.1111G>A ENSP00000306923.3:p.Gly371Arg
ENST00000315987.6:c.1111G>A ENSP00000319591.2:p.Gly371Arg
ENST00000369697.5:c.1111G>A ENSP00000358711.1:p.Gly371Arg
NM_004980.4:c.1111G>A , LRG_445t1:c.1111G>A NP_004971.2:p.Gly371Arg
NM_172198.2:c.1111G>A NP_751948.1:p.Gly371Arg
XM_005270851.3:c.1111G>A XP_005270908.1:p.Gly371Arg
XM_006710629.2:c.1111G>A XP_006710692.1:p.Gly371Arg
XM_006710630.2:c.1111G>A XP_006710693.1:p.Gly371Arg
XM_006710631.2:c.1111G>A XP_006710694.1:p.Gly371Arg
XM_005270851.4:c.1111G>A XP_005270908.1:p.Gly371Arg
XM_006710629.4:c.1111G>A XP_006710692.1:p.Gly371Arg
XM_006710630.3:c.1111G>A XP_006710693.1:p.Gly371Arg
XM_006710631.3:c.1111G>A XP_006710694.1:p.Gly371Arg
XM_017001244.2:c.1111G>A XP_016856733.1:p.Gly371Arg
NM_001378969.1:c.1111G>A MANE Select NP_001365898.1:p.Gly371Arg
NM_001378970.1:c.1111G>A NP_001365899.1:p.Gly371Arg
NM_004980.5:c.1111G>A NP_004971.2:p.Gly371Arg
NM_172198.3:c.1111G>A NP_751948.1:p.Gly371Arg
Search 100 bp 5'
Search 100 bp 3'