Canonical Allele Identifier: CA1752428166

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947207T= , CM000669.2:g.150947207T=	GRCh38
NC_000007.13:g.150644295T= , CM000669.1:g.150644295T=	GRCh37
NC_000007.12:g.150275228T=	NCBI36
NG_008916.1:g.35720A= , LRG_288:g.35720A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3985+121A=
ENST00000262186.10:c.3152+121A= MANE Select	ENSP00000262186.5:n.3152+121A=
ENST00000330883.9:c.2132+121A=	ENSP00000328531.4:n.2132+121A=
ENST00000262186.9:c.3152+121A=	ENSP00000262186.5:n.3152+121A=
ENST00000330883.8:c.2132+121A=	ENSP00000328531.4:n.2132+121A=
NM_000238.3:c.3152+121A= , LRG_288t1:c.3152+121A=	NP_000229.1:n.3152+121A=
NM_172057.2:c.2132+121A= , LRG_288t3:c.2132+121A=	NP_742054.1:n.2132+121A=
XM_011516185.1:c.2852+121A=	XP_011514487.1:n.2852+121A=
XM_011516185.2:c.2852+121A=	XP_011514487.1:n.2852+121A=
XM_017012195.1:c.3002+121A=	XP_016867684.1:n.3002+121A=
XM_017012196.1:c.2975+121A=	XP_016867685.1:n.2975+121A=
NM_000238.4:c.3152+121A= MANE Select	NP_000229.1:n.3152+121A=
NM_172057.3:c.2132+121A=	NP_742054.1:n.2132+121A=