Canonical Allele Identifier: CA1007498
Gene: KCND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 393083
dbSNP Id: rs774338559

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111786957C>T , CM000663.2:g.111786957C>T GRCh38
NC_000001.10:g.112329579C>T , CM000663.1:g.112329579C>T GRCh37
NC_000001.9:g.112131102C>T NCBI36
NG_032011.2:g.207199G>A , LRG_445:g.207199G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302127.5:c.1256G>A MANE Select ENSP00000306923.4:p.Arg419His
ENST00000302127.4:c.1256G>A ENSP00000306923.3:p.Arg419His
ENST00000315987.6:c.1256G>A ENSP00000319591.2:p.Arg419His
ENST00000369697.5:c.1256G>A ENSP00000358711.1:p.Arg419His
NM_004980.4:c.1256G>A , LRG_445t1:c.1256G>A NP_004971.2:p.Arg419His
NM_172198.2:c.1256G>A NP_751948.1:p.Arg419His
XM_005270851.3:c.1256G>A XP_005270908.1:p.Arg419His
XM_006710629.2:c.1256G>A XP_006710692.1:p.Arg419His
XM_006710630.2:c.1256G>A XP_006710693.1:p.Arg419His
XM_006710631.2:c.1256G>A XP_006710694.1:p.Arg419His
XM_005270851.4:c.1256G>A XP_005270908.1:p.Arg419His
XM_006710629.4:c.1256G>A XP_006710692.1:p.Arg419His
XM_006710630.3:c.1256G>A XP_006710693.1:p.Arg419His
XM_006710631.3:c.1256G>A XP_006710694.1:p.Arg419His
XM_017001244.2:c.1256G>A XP_016856733.1:p.Arg419His
NM_001378969.1:c.1256G>A MANE Select NP_001365898.1:p.Arg419His
NM_001378970.1:c.1256G>A NP_001365899.1:p.Arg419His
NM_004980.5:c.1256G>A NP_004971.2:p.Arg419His
NM_172198.3:c.1256G>A NP_751948.1:p.Arg419His