Canonical Allele Identifier: CA16622032

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649796G>A (hg19) ; chr7:g.150952708G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952708G>A , CM000669.2:g.150952708G>A	GRCh38
NC_000007.13:g.150649796G>A , CM000669.1:g.150649796G>A	GRCh37
NC_000007.12:g.150280729G>A	NCBI36
NG_008916.1:g.30219C>T , LRG_288:g.30219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.572C>T
ENST00000684116.1:n.167C>T
ENST00000684241.1:n.2107C>T
ENST00000262186.10:c.1274C>T MANE Select	ENSP00000262186.5:p.Thr425Ile
ENST00000330883.9:c.254C>T	ENSP00000328531.4:p.Thr85Ile
ENST00000262186.9:c.1274C>T	ENSP00000262186.5:p.Thr425Ile
ENST00000330883.8:c.254C>T	ENSP00000328531.4:p.Thr85Ile
ENST00000430723.4:c.926C>T	ENSP00000387657.4:p.Thr309Ile
ENST00000461280.1:n.561C>T
ENST00000473610.5:n.579C>T
ENST00000532957.5:n.1497C>T
NM_000238.3:c.1274C>T , LRG_288t1:c.1274C>T	NP_000229.1:p.Thr425Ile
NM_001204798.1:c.254C>T	NP_001191727.1:p.Thr85Ile
NM_172056.2:c.1274C>T , LRG_288t2:c.1274C>T	NP_742053.1:p.Thr425Ile
NM_172057.2:c.254C>T , LRG_288t3:c.254C>T	NP_742054.1:p.Thr85Ile
XM_011516185.1:c.974C>T	XP_011514487.1:p.Thr325Ile
XM_011516186.1:c.1274C>T	XP_011514488.1:p.Thr425Ile
XM_011516185.2:c.974C>T	XP_011514487.1:p.Thr325Ile
XM_011516186.3:c.1274C>T	XP_011514488.1:p.Thr425Ile
XM_017012195.1:c.1124C>T	XP_016867684.1:p.Thr375Ile
XM_017012196.1:c.1097C>T	XP_016867685.1:p.Thr366Ile
NM_000238.4:c.1274C>T MANE Select	NP_000229.1:p.Thr425Ile
NM_001204798.2:c.254C>T	NP_001191727.1:p.Thr85Ile
NM_172057.3:c.254C>T	NP_742054.1:p.Thr85Ile