Canonical Allele Identifier: CA10964747

Gene: KCND3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111867858A>C , CM000663.2:g.111867858A>C	GRCh38
NC_000001.10:g.112410480A>C , CM000663.1:g.112410480A>C	GRCh37
NC_000001.9:g.112212003A>C	NCBI36
NG_032011.2:g.126298T>G , LRG_445:g.126298T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703641.1:n.1606-26010T>G
ENST00000703642.1:n.1412-26513T>G
ENST00000302127.5:c.1107-80752T>G MANE Select	ENSP00000306923.4:n.1107-80752T>G
ENST00000302127.4:c.1107-80752T>G	ENSP00000306923.3:n.1107-80752T>G
ENST00000315987.6:c.1107-80752T>G	ENSP00000319591.2:n.1107-80752T>G
ENST00000369697.5:c.1107-80752T>G	ENSP00000358711.1:n.1107-80752T>G
NM_004980.4:c.1107-80752T>G , LRG_445t1:c.1107-80752T>G	NP_004971.2:n.1107-80752T>G
NM_172198.2:c.1107-80752T>G	NP_751948.1:n.1107-80752T>G
XM_005270851.3:c.1107-80752T>G	XP_005270908.1:n.1107-80752T>G
XM_006710629.2:c.1107-80752T>G	XP_006710692.1:n.1107-80752T>G
XM_006710630.2:c.1107-80752T>G	XP_006710693.1:n.1107-80752T>G
XM_006710631.2:c.1107-80752T>G	XP_006710694.1:n.1107-80752T>G
XM_011541427.1:c.1107-36727T>G	XP_011539729.1:n.1107-36727T>G
XM_005270851.4:c.1107-80752T>G	XP_005270908.1:n.1107-80752T>G
XM_006710629.4:c.1107-80752T>G	XP_006710692.1:n.1107-80752T>G
XM_006710630.3:c.1107-80752T>G	XP_006710693.1:n.1107-80752T>G
XM_006710631.3:c.1107-80752T>G	XP_006710694.1:n.1107-80752T>G
XM_011541427.3:c.1107-36727T>G	XP_011539729.1:n.1107-36727T>G
XM_017001244.2:c.1107-80752T>G	XP_016856733.1:n.1107-80752T>G
NM_001378969.1:c.1107-80752T>G MANE Select	NP_001365898.1:n.1107-80752T>G
NM_001378970.1:c.1107-80752T>G	NP_001365899.1:n.1107-80752T>G
NM_004980.5:c.1107-80752T>G	NP_004971.2:n.1107-80752T>G
NM_172198.3:c.1107-80752T>G	NP_751948.1:n.1107-80752T>G