Canonical Allele Identifier: CA369853724

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645570C>A (hg19) ; chr7:g.150948482C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948482C>A , CM000669.2:g.150948482C>A	GRCh38
NC_000007.13:g.150645570C>A , CM000669.1:g.150645570C>A	GRCh37
NC_000007.12:g.150276503C>A	NCBI36
NG_008916.1:g.34445G>T , LRG_288:g.34445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3487G>T
ENST00000262186.10:c.2654G>T MANE Select	ENSP00000262186.5:p.Arg885Leu
ENST00000330883.9:c.1634G>T	ENSP00000328531.4:p.Arg545Leu
ENST00000262186.9:c.2654G>T	ENSP00000262186.5:p.Arg885Leu
ENST00000330883.8:c.1634G>T	ENSP00000328531.4:p.Arg545Leu
NM_000238.3:c.2654G>T , LRG_288t1:c.2654G>T	NP_000229.1:p.Arg885Leu
NM_172057.2:c.1634G>T , LRG_288t3:c.1634G>T	NP_742054.1:p.Arg545Leu
XM_011516185.1:c.2354G>T	XP_011514487.1:p.Arg785Leu
XM_011516186.1:c.2654G>T	XP_011514488.1:p.Arg885Leu
XM_011516185.2:c.2354G>T	XP_011514487.1:p.Arg785Leu
XM_011516186.3:c.2654G>T	XP_011514488.1:p.Arg885Leu
XM_017012195.1:c.2504G>T	XP_016867684.1:p.Arg835Leu
XM_017012196.1:c.2477G>T	XP_016867685.1:p.Arg826Leu
NM_000238.4:c.2654G>T MANE Select	NP_000229.1:p.Arg885Leu
NM_172057.3:c.1634G>T	NP_742054.1:p.Arg545Leu