Canonical Allele Identifier: CA1955302212

Gene: KCNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17774564A= , CM000673.2:g.17774564A=	GRCh38
NC_000011.9:g.17796111A= , CM000673.1:g.17796111A=	GRCh37
NC_000011.8:g.17752687A=	NCBI36
NG_041827.1:g.43617A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001112741.2:c.1504+1966A= MANE Select	NP_001106212.1:n.1504+1966A=
ENST00000265969.8:c.1504+1966A= MANE Select	ENSP00000265969.7:n.1504+1966A=
NM_001112741.1:c.1504+1966A=	NP_001106212.1:n.1504+1966A=
NM_004976.4:c.*1934A=	NP_004967.1:n.*1934A=
ENST00000265969.6:c.1504+1966A=	ENSP00000265969.6:n.1504+1966A=
ENST00000379472.3:c.*1934A=	ENSP00000368785.3:n.*1934A=
ENST00000379472.4:c.*1934A=	ENSP00000368785.3:n.*1934A=
ENST00000525802.1:n.280+734A=
ENST00000638366.1:c.222+734A=	ENSP00000491016.1:n.222+734A=
ENST00000638395.1:n.205+734A=
ENST00000638825.1:c.41+1966A=
ENST00000639325.2:c.1504+1966A=	ENSP00000492663.2:n.1504+1966A=
ENST00000639495.1:c.408+1966A=
ENST00000640318.2:c.1504+1966A=	ENSP00000491189.2:n.1504+1966A=
ENST00000640461.1:c.72+1966A=
ENST00000640909.2:c.1504+1966A=	ENSP00000491644.2:n.1504+1966A=
ENST00000675775.1:c.1504+1966A=	ENSP00000502716.1:n.1504+1966A=
XM_011520078.1:c.1504+1966A=	XP_011518380.1:n.1504+1966A=
XM_011520079.1:c.1504+1966A=	XP_011518381.1:n.1504+1966A=
XM_011520080.1:c.1566+734A=	XP_011518382.1:n.1566+734A=
XM_011520081.1:c.1504+1966A=	XP_011518383.1:n.1504+1966A=