Canonical Allele Identifier: CA5906672

Gene: KCNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17736437C>A , CM000673.2:g.17736437C>A	GRCh38
NC_000011.9:g.17757984C>A , CM000673.1:g.17757984C>A	GRCh37
NC_000011.8:g.17714560C>A	NCBI36
NG_041827.1:g.5490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265969.8:c.435C>A MANE Select	ENSP00000265969.7:p.Gly145=
ENST00000379472.4:c.435C>A	ENSP00000368785.3:p.Gly145=
ENST00000639325.2:c.435C>A	ENSP00000492663.2:p.Gly145=
ENST00000640318.2:c.435C>A	ENSP00000491189.2:p.Gly145=
ENST00000640909.2:c.435C>A	ENSP00000491644.2:p.Gly145=
ENST00000675775.1:c.435C>A	ENSP00000502716.1:p.Gly145=
ENST00000265969.6:c.435C>A	ENSP00000265969.6:p.Gly145=
ENST00000379472.3:c.435C>A	ENSP00000368785.3:p.Gly145=
NM_001112741.1:c.435C>A	NP_001106212.1:p.Gly145=
NM_004976.4:c.435C>A	NP_004967.1:p.Gly145=
XM_011520078.1:c.435C>A	XP_011518380.1:p.Gly145=
XM_011520079.1:c.435C>A	XP_011518381.1:p.Gly145=
XM_011520080.1:c.435C>A	XP_011518382.1:p.Gly145=
XM_011520081.1:c.435C>A	XP_011518383.1:p.Gly145=
XR_930866.1:n.528C>A
XR_930866.2:n.1628C>A
NM_001112741.2:c.435C>A MANE Select	NP_001106212.1:p.Gly145=