Canonical Allele Identifier: CA473519401

Gene: KCNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17736152G>C , CM000673.2:g.17736152G>C	GRCh38
NC_000011.9:g.17757699G>C , CM000673.1:g.17757699G>C	GRCh37
NC_000011.8:g.17714275G>C	NCBI36
NG_041827.1:g.5205G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265969.8:c.150G>C MANE Select	ENSP00000265969.7:p.Pro50=
ENST00000379472.4:c.150G>C	ENSP00000368785.3:p.Pro50=
ENST00000639325.2:c.150G>C	ENSP00000492663.2:p.Pro50=
ENST00000640318.2:c.150G>C	ENSP00000491189.2:p.Pro50=
ENST00000640909.2:c.150G>C	ENSP00000491644.2:p.Pro50=
ENST00000675775.1:c.150G>C	ENSP00000502716.1:p.Pro50=
ENST00000265969.6:c.150G>C	ENSP00000265969.6:p.Pro50=
ENST00000379472.3:c.150G>C	ENSP00000368785.3:p.Pro50=
NM_001112741.1:c.150G>C	NP_001106212.1:p.Pro50=
NM_004976.4:c.150G>C	NP_004967.1:p.Pro50=
XM_011520078.1:c.150G>C	XP_011518380.1:p.Pro50=
XM_011520079.1:c.150G>C	XP_011518381.1:p.Pro50=
XM_011520080.1:c.150G>C	XP_011518382.1:p.Pro50=
XM_011520081.1:c.150G>C	XP_011518383.1:p.Pro50=
XR_930866.1:n.243G>C
XR_930866.2:n.1343G>C
NM_001112741.2:c.150G>C MANE Select	NP_001106212.1:p.Pro50=