Canonical Allele Identifier: CA1189061652

Gene: KCND3

Linked Data

• ClinVar Variation Id: 2154736
• ClinVar RCV Id: RCV003081932
• dbSNP Id: rs1571620165

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111776295T>G , CM000663.2:g.111776295T>G	GRCh38
NC_000001.10:g.112318917T>G , CM000663.1:g.112318917T>G	GRCh37
NC_000001.9:g.112120440T>G	NCBI36
NG_032011.2:g.217861A>C , LRG_445:g.217861A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302127.5:c.1767-17A>C MANE Select	ENSP00000306923.4:n.1767-17A>C
ENST00000302127.4:c.1710-17A>C	ENSP00000306923.3:n.1710-17A>C
ENST00000315987.6:c.1767-17A>C	ENSP00000319591.2:n.1767-17A>C
ENST00000369697.5:c.1710-17A>C	ENSP00000358711.1:n.1710-17A>C
NM_004980.4:c.1767-17A>C , LRG_445t1:c.1767-17A>C	NP_004971.2:n.1767-17A>C
NM_172198.2:c.1710-17A>C	NP_751948.1:n.1710-17A>C
XM_005270851.3:c.1767-17A>C	XP_005270908.1:n.1767-17A>C
XM_006710629.2:c.1767-17A>C	XP_006710692.1:n.1767-17A>C
XM_006710630.2:c.1710-17A>C	XP_006710693.1:n.1710-17A>C
XM_006710631.2:c.1519-17A>C	XP_006710694.1:n.1519-17A>C
XM_005270851.4:c.1767-17A>C	XP_005270908.1:n.1767-17A>C
XM_006710629.4:c.1767-17A>C	XP_006710692.1:n.1767-17A>C
XM_006710630.3:c.1710-17A>C	XP_006710693.1:n.1710-17A>C
XM_006710631.3:c.1519-17A>C	XP_006710694.1:n.1519-17A>C
XM_017001244.2:c.1767-17A>C	XP_016856733.1:n.1767-17A>C
NM_001378969.1:c.1767-17A>C MANE Select	NP_001365898.1:n.1767-17A>C
NM_001378970.1:c.1710-17A>C	NP_001365899.1:n.1710-17A>C
NM_004980.5:c.1767-17A>C	NP_004971.2:n.1767-17A>C
NM_172198.3:c.1710-17A>C	NP_751948.1:n.1710-17A>C