Canonical Allele Identifier: CA406968260

Gene: KCNC3

Linked Data

• MyVariant Identifiers: chr19:g.50823850C>T (hg19) ; chr19:g.50320593C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50320593C>T , CM000681.2:g.50320593C>T	GRCh38
NC_000019.9:g.50823850C>T , CM000681.1:g.50823850C>T	GRCh37
NC_000019.8:g.55515662C>T	NCBI36
NG_008134.2:g.13785G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477616.2:c.2170G>A MANE Select	ENSP00000434241.1:p.Ala724Thr
ENST00000670667.1:c.2170G>A	ENSP00000499301.1:p.Gly724Ser
ENST00000376959.6:c.2170G>A	ENSP00000366158.2:p.Ala724Thr
ENST00000474951.1:c.118G>A	ENSP00000432438.1:p.Ala40Thr
ENST00000477616.1:c.2170G>A	ENSP00000434241.1:p.Ala724Thr
NM_004977.2:c.2170G>A	NP_004968.2:p.Ala724Thr
NR_110912.1:n.239G>A
XM_006723203.2:c.2170G>A	XP_006723266.1:p.Ala724Thr
XM_011526925.1:c.2170G>A	XP_011525227.1:p.Gly724Ser
XM_011526926.1:c.2170G>A	XP_011525228.1:p.Ala724Thr
XM_011526927.1:c.2170G>A	XP_011525229.1:p.Ala724Thr
XM_011526928.1:c.2170G>A	XP_011525230.1:p.Ala724Thr
NM_001372305.1:c.1942G>A	NP_001359234.1:p.Ala648Thr
NM_004977.3:c.2170G>A MANE Select	NP_004968.2:p.Ala724Thr
NR_110912.2:n.260G>A