Canonical Allele Identifier: CA1955301254

Gene: KCNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17772355G= , CM000673.2:g.17772355G=	GRCh38
NC_000011.9:g.17793902G= , CM000673.1:g.17793902G=	GRCh37
NC_000011.8:g.17750478G=	NCBI36
NG_041827.1:g.41408G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265969.8:c.1261G= MANE Select	ENSP00000265969.7:p.Ala421=
ENST00000379472.4:c.1261G=	ENSP00000368785.3:p.Ala421=
ENST00000639325.2:c.1261G=	ENSP00000492663.2:p.Ala421=
ENST00000639495.1:c.165G=
ENST00000640153.1:n.789G=
ENST00000640318.2:c.1261G=	ENSP00000491189.2:p.Ala421=
ENST00000640909.2:c.1261G=	ENSP00000491644.2:p.Ala421=
ENST00000675775.1:c.1261G=	ENSP00000502716.1:p.Ala421=
ENST00000265969.6:c.1261G=	ENSP00000265969.6:p.Ala421=
ENST00000379472.3:c.1261G=	ENSP00000368785.3:p.Ala421=
NM_001112741.1:c.1261G=	NP_001106212.1:p.Ala421=
NM_004976.4:c.1261G=	NP_004967.1:p.Ala421=
XM_011520078.1:c.1261G=	XP_011518380.1:p.Ala421=
XM_011520079.1:c.1261G=	XP_011518381.1:p.Ala421=
XM_011520080.1:c.1261G=	XP_011518382.1:p.Ala421=
XM_011520081.1:c.1261G=	XP_011518383.1:p.Ala421=
XR_930866.1:n.1354G=
XR_930866.2:n.2454G=
NM_001112741.2:c.1261G= MANE Select	NP_001106212.1:p.Ala421=