Canonical Allele Identifier: CA369860000

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649754C>A (hg19) ; chr7:g.150952666C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952666C>A , CM000669.2:g.150952666C>A	GRCh38
NC_000007.13:g.150649754C>A , CM000669.1:g.150649754C>A	GRCh37
NC_000007.12:g.150280687C>A	NCBI36
NG_008916.1:g.30261G>T , LRG_288:g.30261G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.614G>T
ENST00000684116.1:n.209G>T
ENST00000684241.1:n.2149G>T
ENST00000262186.10:c.1316G>T MANE Select	ENSP00000262186.5:p.Gly439Val
ENST00000330883.9:c.296G>T	ENSP00000328531.4:p.Gly99Val
ENST00000262186.9:c.1316G>T	ENSP00000262186.5:p.Gly439Val
ENST00000330883.8:c.296G>T	ENSP00000328531.4:p.Gly99Val
ENST00000430723.4:c.968G>T	ENSP00000387657.4:p.Gly323Val
ENST00000461280.1:n.603G>T
ENST00000473610.5:n.621G>T
ENST00000532957.5:n.1539G>T
NM_000238.3:c.1316G>T , LRG_288t1:c.1316G>T	NP_000229.1:p.Gly439Val
NM_001204798.1:c.296G>T	NP_001191727.1:p.Gly99Val
NM_172056.2:c.1316G>T , LRG_288t2:c.1316G>T	NP_742053.1:p.Gly439Val
NM_172057.2:c.296G>T , LRG_288t3:c.296G>T	NP_742054.1:p.Gly99Val
XM_011516185.1:c.1016G>T	XP_011514487.1:p.Gly339Val
XM_011516186.1:c.1316G>T	XP_011514488.1:p.Gly439Val
XM_011516185.2:c.1016G>T	XP_011514487.1:p.Gly339Val
XM_011516186.3:c.1316G>T	XP_011514488.1:p.Gly439Val
XM_017012195.1:c.1166G>T	XP_016867684.1:p.Gly389Val
XM_017012196.1:c.1139G>T	XP_016867685.1:p.Gly380Val
NM_000238.4:c.1316G>T MANE Select	NP_000229.1:p.Gly439Val
NM_001204798.2:c.296G>T	NP_001191727.1:p.Gly99Val
NM_172057.3:c.296G>T	NP_742054.1:p.Gly99Val