Canonical Allele Identifier: CA1752430110

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947717G= , CM000669.2:g.150947717G=	GRCh38
NC_000007.13:g.150644805G= , CM000669.1:g.150644805G=	GRCh37
NC_000007.12:g.150275738G=	NCBI36
NG_008916.1:g.35210C= , LRG_288:g.35210C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3687C=
ENST00000262186.10:c.2854C= MANE Select	ENSP00000262186.5:p.Pro952=
ENST00000330883.9:c.1834C=	ENSP00000328531.4:p.Pro612=
ENST00000262186.9:c.2854C=	ENSP00000262186.5:p.Pro952=
ENST00000330883.8:c.1834C=	ENSP00000328531.4:p.Pro612=
NM_000238.3:c.2854C= , LRG_288t1:c.2854C=	NP_000229.1:p.Pro952=
NM_172057.2:c.1834C= , LRG_288t3:c.1834C=	NP_742054.1:p.Pro612=
XM_011516185.1:c.2554C=	XP_011514487.1:p.Pro852=
XM_011516186.1:c.2693-26C=	XP_011514488.1:n.2693-26C=
XM_011516185.2:c.2554C=	XP_011514487.1:p.Pro852=
XM_011516186.3:c.2693-26C=	XP_011514488.1:n.2693-26C=
XM_017012195.1:c.2704C=	XP_016867684.1:p.Pro902=
XM_017012196.1:c.2677C=	XP_016867685.1:p.Pro893=
NM_000238.4:c.2854C= MANE Select	NP_000229.1:p.Pro952=
NM_172057.3:c.1834C=	NP_742054.1:p.Pro612=