Canonical Allele Identifier: CA419707956

Gene: KCND3

Linked Data

• MyVariant Identifiers: chr1:g.112524548G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111981926G>T , CM000663.2:g.111981926G>T	GRCh38
NC_000001.10:g.112524548G>T , CM000663.1:g.112524548G>T	GRCh37
NC_000001.9:g.112326071G>T	NCBI36
NG_032011.2:g.12230C>A , LRG_445:g.12230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703641.1:n.1300C>A
ENST00000703642.1:n.1106C>A
ENST00000703643.1:n.1103C>A
ENST00000302127.5:c.801C>A MANE Select	ENSP00000306923.4:p.Ile267=
ENST00000302127.4:c.801C>A	ENSP00000306923.3:p.Ile267=
ENST00000315987.6:c.801C>A	ENSP00000319591.2:p.Ile267=
ENST00000369697.5:c.801C>A	ENSP00000358711.1:p.Ile267=
NM_004980.4:c.801C>A , LRG_445t1:c.801C>A	NP_004971.2:p.Ile267=
NM_172198.2:c.801C>A	NP_751948.1:p.Ile267=
XM_005270851.3:c.801C>A	XP_005270908.1:p.Ile267=
XM_006710629.2:c.801C>A	XP_006710692.1:p.Ile267=
XM_006710630.2:c.801C>A	XP_006710693.1:p.Ile267=
XM_006710631.2:c.801C>A	XP_006710694.1:p.Ile267=
XM_006710632.2:c.801C>A	XP_006710695.1:p.Ile267=
XM_011541425.1:c.801C>A	XP_011539727.1:p.Ile267=
XM_011541426.1:c.801C>A	XP_011539728.1:p.Ile267=
XM_011541427.1:c.801C>A	XP_011539729.1:p.Ile267=
XM_011541428.1:c.801C>A	XP_011539730.1:p.Ile267=
XM_005270851.4:c.801C>A	XP_005270908.1:p.Ile267=
XM_006710629.4:c.801C>A	XP_006710692.1:p.Ile267=
XM_006710630.3:c.801C>A	XP_006710693.1:p.Ile267=
XM_006710631.3:c.801C>A	XP_006710694.1:p.Ile267=
XM_006710632.3:c.801C>A	XP_006710695.1:p.Ile267=
XM_011541425.3:c.801C>A	XP_011539727.1:p.Ile267=
XM_011541426.2:c.801C>A	XP_011539728.1:p.Ile267=
XM_011541427.3:c.801C>A	XP_011539729.1:p.Ile267=
XM_011541428.2:c.801C>A	XP_011539730.1:p.Ile267=
XM_017001244.2:c.801C>A	XP_016856733.1:p.Ile267=
XM_017001245.2:c.801C>A	XP_016856734.1:p.Ile267=
NM_001378969.1:c.801C>A MANE Select	NP_001365898.1:p.Ile267=
NM_001378970.1:c.801C>A	NP_001365899.1:p.Ile267=
NM_004980.5:c.801C>A	NP_004971.2:p.Ile267=
NM_172198.3:c.801C>A	NP_751948.1:p.Ile267=