Canonical Allele Identifier: CA406956938

Gene: KCNC3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50329049C>A , CM000681.2:g.50329049C>A	GRCh38
NC_000019.9:g.50832306C>A , CM000681.1:g.50832306C>A	GRCh37
NC_000019.8:g.55524118C>A	NCBI36
NG_008134.2:g.5329G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004977.3:c.34G>T MANE Select	NP_004968.2:p.Gly12Trp
ENST00000477616.2:c.34G>T MANE Select	ENSP00000434241.1:p.Gly12Trp
NM_001372305.1:c.-195G>T	NP_001359234.1:n.-195G>T
NM_004977.2:c.34G>T	NP_004968.2:p.Gly12Trp
NR_110912.1:n.47+4420G>T
NR_110912.2:n.68+4420G>T
ENST00000376959.6:c.34G>T	ENSP00000366158.2:p.Gly12Trp
ENST00000474951.1:c.-75+4420G>T	ENSP00000432438.1:n.-75+4420G>T
ENST00000477616.1:c.34G>T	ENSP00000434241.1:p.Gly12Trp
ENST00000670667.1:c.34G>T	ENSP00000499301.1:p.Gly12Trp
XM_006723203.2:c.34G>T	XP_006723266.1:p.Gly12Trp
XM_011526925.1:c.34G>T	XP_011525227.1:p.Gly12Trp
XM_011526926.1:c.34G>T	XP_011525228.1:p.Gly12Trp
XM_011526927.1:c.34G>T	XP_011525229.1:p.Gly12Trp
XM_011526928.1:c.34G>T	XP_011525230.1:p.Gly12Trp