Canonical Allele Identifier: CA1189108630

Gene: KCND3

Linked Data

• dbSNP Id: rs2798334

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111894722T>A , CM000663.2:g.111894722T>A	GRCh38
NC_000001.10:g.112437344T>A , CM000663.1:g.112437344T>A	GRCh37
NC_000001.9:g.112238867T>A	NCBI36
NG_032011.2:g.99434A>T , LRG_445:g.99434A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703641.1:n.1606-52874A>T
ENST00000703642.1:n.1412-53377A>T
ENST00000302127.5:c.1106+86899A>T MANE Select	ENSP00000306923.4:n.1106+86899A>T
ENST00000302127.4:c.1106+86899A>T	ENSP00000306923.3:n.1106+86899A>T
ENST00000315987.6:c.1106+86899A>T	ENSP00000319591.2:n.1106+86899A>T
ENST00000369697.5:c.1106+86899A>T	ENSP00000358711.1:n.1106+86899A>T
NM_004980.4:c.1106+86899A>T , LRG_445t1:c.1106+86899A>T	NP_004971.2:n.1106+86899A>T
NM_172198.2:c.1106+86899A>T	NP_751948.1:n.1106+86899A>T
XM_005270851.3:c.1106+86899A>T	XP_005270908.1:n.1106+86899A>T
XM_006710629.2:c.1106+86899A>T	XP_006710692.1:n.1106+86899A>T
XM_006710630.2:c.1106+86899A>T	XP_006710693.1:n.1106+86899A>T
XM_006710631.2:c.1106+86899A>T	XP_006710694.1:n.1106+86899A>T
XM_011541427.1:c.1107-63591A>T	XP_011539729.1:n.1107-63591A>T
XM_005270851.4:c.1106+86899A>T	XP_005270908.1:n.1106+86899A>T
XM_006710629.4:c.1106+86899A>T	XP_006710692.1:n.1106+86899A>T
XM_006710630.3:c.1106+86899A>T	XP_006710693.1:n.1106+86899A>T
XM_006710631.3:c.1106+86899A>T	XP_006710694.1:n.1106+86899A>T
XM_011541427.3:c.1107-63591A>T	XP_011539729.1:n.1107-63591A>T
XM_017001244.2:c.1106+86899A>T	XP_016856733.1:n.1106+86899A>T
NM_001378969.1:c.1106+86899A>T MANE Select	NP_001365898.1:n.1106+86899A>T
NM_001378970.1:c.1106+86899A>T	NP_001365899.1:n.1106+86899A>T
NM_004980.5:c.1106+86899A>T	NP_004971.2:n.1106+86899A>T
NM_172198.3:c.1106+86899A>T	NP_751948.1:n.1106+86899A>T