Canonical Allele Identifier: CA1752429780

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947620C= , CM000669.2:g.150947620C=	GRCh38
NC_000007.13:g.150644708C= , CM000669.1:g.150644708C=	GRCh37
NC_000007.12:g.150275641C=	NCBI36
NG_008916.1:g.35307G= , LRG_288:g.35307G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3784G=
ENST00000262186.10:c.2951G= MANE Select	ENSP00000262186.5:p.Cys984=
ENST00000330883.9:c.1931G=	ENSP00000328531.4:p.Cys644=
ENST00000262186.9:c.2951G=	ENSP00000262186.5:p.Cys984=
ENST00000330883.8:c.1931G=	ENSP00000328531.4:p.Cys644=
NM_000238.3:c.2951G= , LRG_288t1:c.2951G=	NP_000229.1:p.Cys984=
NM_172057.2:c.1931G= , LRG_288t3:c.1931G=	NP_742054.1:p.Cys644=
XM_011516185.1:c.2651G=	XP_011514487.1:p.Cys884=
XM_011516186.1:c.*31G=	XP_011514488.1:n.*31G=
XM_011516185.2:c.2651G=	XP_011514487.1:p.Cys884=
XM_011516186.3:c.*31G=	XP_011514488.1:n.*31G=
XM_017012195.1:c.2801G=	XP_016867684.1:p.Cys934=
XM_017012196.1:c.2774G=	XP_016867685.1:p.Cys925=
NM_000238.4:c.2951G= MANE Select	NP_000229.1:p.Cys984=
NM_172057.3:c.1931G=	NP_742054.1:p.Cys644=