Canonical Allele Identifier: CA1752431866

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948883G= , CM000669.2:g.150948883G=	GRCh38
NC_000007.13:g.150645971G= , CM000669.1:g.150645971G=	GRCh37
NC_000007.12:g.150276904G=	NCBI36
NG_008916.1:g.34044C= , LRG_288:g.34044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3398C=
ENST00000262186.10:c.2565C= MANE Select	ENSP00000262186.5:p.Ser855=
ENST00000330883.9:c.1545C=	ENSP00000328531.4:p.Ser515=
ENST00000262186.9:c.2565C=	ENSP00000262186.5:p.Ser855=
ENST00000330883.8:c.1545C=	ENSP00000328531.4:p.Ser515=
NM_000238.3:c.2565C= , LRG_288t1:c.2565C=	NP_000229.1:p.Ser855=
NM_172057.2:c.1545C= , LRG_288t3:c.1545C=	NP_742054.1:p.Ser515=
XM_011516185.1:c.2265C=	XP_011514487.1:p.Ser755=
XM_011516186.1:c.2565C=	XP_011514488.1:p.Ser855=
XM_011516185.2:c.2265C=	XP_011514487.1:p.Ser755=
XM_011516186.3:c.2565C=	XP_011514488.1:p.Ser855=
XM_017012195.1:c.2415C=	XP_016867684.1:p.Ser805=
XM_017012196.1:c.2388C=	XP_016867685.1:p.Ser796=
NM_000238.4:c.2565C= MANE Select	NP_000229.1:p.Ser855=
NM_172057.3:c.1545C=	NP_742054.1:p.Ser515=