Canonical Allele Identifier: CA458871529

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648693G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951605G>T , CM000669.2:g.150951605G>T	GRCh38
NC_000007.13:g.150648693G>T , CM000669.1:g.150648693G>T	GRCh37
NC_000007.12:g.150279626G>T	NCBI36
NG_008916.1:g.31322C>A , LRG_288:g.31322C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1086C>A
ENST00000684241.1:n.2621C>A
ENST00000262186.10:c.1788C>A MANE Select	ENSP00000262186.5:p.Pro596=
ENST00000330883.9:c.768C>A	ENSP00000328531.4:p.Pro256=
ENST00000262186.9:c.1788C>A	ENSP00000262186.5:p.Pro596=
ENST00000330883.8:c.768C>A	ENSP00000328531.4:p.Pro256=
ENST00000430723.4:c.1440C>A	ENSP00000387657.4:p.Pro480=
ENST00000461280.1:n.1075C>A
ENST00000473610.5:n.1093C>A
ENST00000532957.5:n.2011C>A
NM_000238.3:c.1788C>A , LRG_288t1:c.1788C>A	NP_000229.1:p.Pro596=
NM_001204798.1:c.768C>A	NP_001191727.1:p.Pro256=
NM_172056.2:c.1788C>A , LRG_288t2:c.1788C>A	NP_742053.1:p.Pro596=
NM_172057.2:c.768C>A , LRG_288t3:c.768C>A	NP_742054.1:p.Pro256=
XM_011516185.1:c.1488C>A	XP_011514487.1:p.Pro496=
XM_011516186.1:c.1788C>A	XP_011514488.1:p.Pro596=
XM_011516185.2:c.1488C>A	XP_011514487.1:p.Pro496=
XM_011516186.3:c.1788C>A	XP_011514488.1:p.Pro596=
XM_017012195.1:c.1638C>A	XP_016867684.1:p.Pro546=
XM_017012196.1:c.1611C>A	XP_016867685.1:p.Pro537=
NM_000238.4:c.1788C>A MANE Select	NP_000229.1:p.Pro596=
NM_001204798.2:c.768C>A	NP_001191727.1:p.Pro256=
NM_172057.3:c.768C>A	NP_742054.1:p.Pro256=