Canonical Allele Identifier: CA9594130

Gene: KCNC3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50320751G>A , CM000681.2:g.50320751G>A	GRCh38
NC_000019.9:g.50824008G>A , CM000681.1:g.50824008G>A	GRCh37
NC_000019.8:g.55515820G>A	NCBI36
NG_008134.2:g.13627C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477616.2:c.2012C>T MANE Select	ENSP00000434241.1:p.Ala671Val
ENST00000670667.1:c.2012C>T	ENSP00000499301.1:p.Ala671Val
ENST00000376959.6:c.2012C>T	ENSP00000366158.2:p.Ala671Val
ENST00000474951.1:c.-41C>T	ENSP00000432438.1:n.-41C>T
ENST00000477616.1:c.2012C>T	ENSP00000434241.1:p.Ala671Val
NM_004977.2:c.2012C>T	NP_004968.2:p.Ala671Val
NR_110912.1:n.81C>T
XM_006723203.2:c.2012C>T	XP_006723266.1:p.Ala671Val
XM_011526925.1:c.2012C>T	XP_011525227.1:p.Ala671Val
XM_011526926.1:c.2012C>T	XP_011525228.1:p.Ala671Val
XM_011526927.1:c.2012C>T	XP_011525229.1:p.Ala671Val
XM_011526928.1:c.2012C>T	XP_011525230.1:p.Ala671Val
NM_001372305.1:c.1784C>T	NP_001359234.1:p.Ala595Val
NM_004977.3:c.2012C>T MANE Select	NP_004968.2:p.Ala671Val
NR_110912.2:n.102C>T