Canonical Allele Identifier: CA28769414

Gene: KCNC4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110227601G>A , CM000663.2:g.110227601G>A	GRCh38
NC_000001.10:g.110770223G>A , CM000663.1:g.110770223G>A	GRCh37
NC_000001.9:g.110571746G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438661.3:c.1819+1423G>A MANE Select	ENSP00000393655.2:n.1819+1423G>A
ENST00000636402.1:c.276-932G>A
ENST00000369787.7:c.1819+1423G>A	ENSP00000358802.3:n.1819+1423G>A
ENST00000412512.2:n.30+15424G>A
ENST00000413138.7:c.1819+1423G>A	ENSP00000388029.3:n.1819+1423G>A
ENST00000438661.2:c.1819+1423G>A	ENSP00000393655.2:n.1819+1423G>A
ENST00000459877.1:n.6463+1423G>A
ENST00000469655.5:c.1819+1423G>A	ENSP00000436656.1:n.1819+1423G>A
NM_001039574.2:c.1819+1423G>A	NP_001034663.1:n.1819+1423G>A
NM_004978.4:c.1819+1423G>A	NP_004969.2:n.1819+1423G>A
NR_036437.1:n.2605+1423G>A
XM_006710625.2:c.1819+1423G>A	XP_006710688.1:n.1819+1423G>A
XM_006710627.2:c.1819+1423G>A	XP_006710690.1:n.1819+1423G>A
XM_011541401.1:c.1819+1423G>A	XP_011539703.1:n.1819+1423G>A
XM_011541402.1:c.882+1423G>A	XP_011539704.1:n.882+1423G>A
XM_011541403.1:c.882+1423G>A	XP_011539705.1:n.882+1423G>A
XM_011541404.1:c.882+1423G>A	XP_011539706.1:n.882+1423G>A
XM_006710625.4:c.1819+1423G>A	XP_006710688.1:n.1819+1423G>A
XM_006710627.4:c.1819+1423G>A	XP_006710690.1:n.1819+1423G>A
XM_011541401.3:c.1819+1423G>A	XP_011539703.1:n.1819+1423G>A
XM_011541402.2:c.882+1423G>A	XP_011539704.1:n.882+1423G>A
XM_011541403.2:c.882+1423G>A	XP_011539705.1:n.882+1423G>A
XM_011541404.2:c.882+1423G>A	XP_011539706.1:n.882+1423G>A
XM_024446790.1:c.1820-932G>A	XP_024302558.1:n.1820-932G>A
NM_001039574.3:c.1819+1423G>A MANE Select	NP_001034663.1:n.1819+1423G>A
NM_001377330.1:c.1819+1423G>A	NP_001364259.1:n.1819+1423G>A
NM_001377331.1:c.882+1423G>A	NP_001364260.1:n.882+1423G>A
NM_004978.6:c.1819+1423G>A	NP_004969.2:n.1819+1423G>A
NR_036437.2:n.3005+1423G>A