Canonical Allele Identifier: CA525503658

Gene: KCND3

Linked Data

• dbSNP Id: rs2798334
• gnomAD v2: 1-112437344-T-G
• MyVariant Identifiers: chr1:g.112437344T>G (hg19) ; chr1:g.111894722T>G (hg38)

Genomic Alleles

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

Transcript Alleles

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