Canonical Allele Identifier: CA1752418159

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958240G= , CM000669.2:g.150958240G=	GRCh38
NC_000007.13:g.150655328G= , CM000669.1:g.150655328G=	GRCh37
NC_000007.12:g.150286261G=	NCBI36
NG_008916.1:g.24687C= , LRG_288:g.24687C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1568C=
ENST00000262186.10:c.735C= MANE Select	ENSP00000262186.5:p.Pro245=
ENST00000262186.9:c.735C=	ENSP00000262186.5:p.Pro245=
ENST00000430723.4:c.387C=	ENSP00000387657.4:p.Pro129=
ENST00000532957.5:n.958C=
NM_000238.3:c.735C= , LRG_288t1:c.735C=	NP_000229.1:p.Pro245=
NM_172056.2:c.735C= , LRG_288t2:c.735C=	NP_742053.1:p.Pro245=
XM_011516185.1:c.435C=	XP_011514487.1:p.Pro145=
XM_011516186.1:c.735C=	XP_011514488.1:p.Pro245=
XM_011516185.2:c.435C=	XP_011514487.1:p.Pro145=
XM_011516186.3:c.735C=	XP_011514488.1:p.Pro245=
XM_017012195.1:c.585C=	XP_016867684.1:p.Pro195=
XM_017012196.1:c.558C=	XP_016867685.1:p.Pro186=
NM_000238.4:c.735C= MANE Select	NP_000229.1:p.Pro245=