Canonical Allele Identifier: CA29311904
Gene: KCND3 HGNC NCBI

Linked Data

dbSNP Id: rs12044963
gnomAD v2: 1-112392360-G-T
gnomAD v3: 1-111849738-G-T
gnomAD v4: 1-111849738-G-T
MyVariant Identifiers: chr1:g.112392360G>T (hg19) chr1:g.111849738G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111849738G>T , CM000663.2:g.111849738G>T GRCh38
NC_000001.10:g.112392360G>T , CM000663.1:g.112392360G>T GRCh37
NC_000001.9:g.112193883G>T NCBI36
NG_032011.2:g.144418C>A , LRG_445:g.144418C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703641.1:n.1606-7890C>A
ENST00000703642.1:n.1412-8393C>A
ENST00000302127.5:c.1107-62632C>A MANE Select ENSP00000306923.4:n.1107-62632C>A
ENST00000302127.4:c.1107-62632C>A ENSP00000306923.3:n.1107-62632C>A
ENST00000315987.6:c.1107-62632C>A ENSP00000319591.2:n.1107-62632C>A
ENST00000369697.5:c.1107-62632C>A ENSP00000358711.1:n.1107-62632C>A
NM_004980.4:c.1107-62632C>A , LRG_445t1:c.1107-62632C>A NP_004971.2:n.1107-62632C>A
NM_172198.2:c.1107-62632C>A NP_751948.1:n.1107-62632C>A
XM_005270851.3:c.1107-62632C>A XP_005270908.1:n.1107-62632C>A
XM_006710629.2:c.1107-62632C>A XP_006710692.1:n.1107-62632C>A
XM_006710630.2:c.1107-62632C>A XP_006710693.1:n.1107-62632C>A
XM_006710631.2:c.1107-62632C>A XP_006710694.1:n.1107-62632C>A
XM_011541427.1:c.1107-18607C>A XP_011539729.1:n.1107-18607C>A
XM_005270851.4:c.1107-62632C>A XP_005270908.1:n.1107-62632C>A
XM_006710629.4:c.1107-62632C>A XP_006710692.1:n.1107-62632C>A
XM_006710630.3:c.1107-62632C>A XP_006710693.1:n.1107-62632C>A
XM_006710631.3:c.1107-62632C>A XP_006710694.1:n.1107-62632C>A
XM_011541427.3:c.1107-18607C>A XP_011539729.1:n.1107-18607C>A
XM_017001244.2:c.1107-62632C>A XP_016856733.1:n.1107-62632C>A
NM_001378969.1:c.1107-62632C>A MANE Select NP_001365898.1:n.1107-62632C>A
NM_001378970.1:c.1107-62632C>A NP_001365899.1:n.1107-62632C>A
NM_004980.5:c.1107-62632C>A NP_004971.2:n.1107-62632C>A
NM_172198.3:c.1107-62632C>A NP_751948.1:n.1107-62632C>A
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