Canonical Allele Identifier: CA1955304667

Gene: KCNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17779621C= , CM000673.2:g.17779621C=	GRCh38
NC_000011.9:g.17801168C= , CM000673.1:g.17801168C=	GRCh37
NC_000011.8:g.17757744C=	NCBI36
NG_041827.1:g.48674C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001112741.2:c.1670C= MANE Select	NP_001106212.1:p.Pro557=
ENST00000265969.8:c.1670C= MANE Select	ENSP00000265969.7:p.Pro557=
NM_001112741.1:c.1670C=	NP_001106212.1:p.Pro557=
ENST00000265969.6:c.1670C=	ENSP00000265969.6:p.Pro557=
ENST00000525802.1:n.446C=
ENST00000526029.1:n.450C=
ENST00000638366.1:c.388C=	ENSP00000491016.1:n.388C=
ENST00000638395.1:n.371C=
ENST00000638825.1:c.207C=
ENST00000639325.2:c.1670C=	ENSP00000492663.2:p.Pro557=
ENST00000639495.1:c.408+7023C=
ENST00000640318.2:c.1670C=	ENSP00000491189.2:p.Pro557=
ENST00000640461.1:c.72+7023C=
ENST00000640909.2:c.1670C=	ENSP00000491644.2:p.Pro557=
ENST00000675775.1:c.1670C=	ENSP00000502716.1:p.Pro557=
XM_011520078.1:c.1504+7023C=	XP_011518380.1:n.1504+7023C=
XM_011520079.1:c.1504+7023C=	XP_011518381.1:n.1504+7023C=