Canonical Allele Identifier: CA369862895

Gene: KCNH2

Linked Data

• gnomAD v3: 7-150958307-G-A
• gnomAD v4: 7-150958307-G-A
• MyVariant Identifiers: chr7:g.150655395G>A (hg19) ; chr7:g.150958307G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958307G>A , CM000669.2:g.150958307G>A	GRCh38
NC_000007.13:g.150655395G>A , CM000669.1:g.150655395G>A	GRCh37
NC_000007.12:g.150286328G>A	NCBI36
NG_008916.1:g.24620C>T , LRG_288:g.24620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1501C>T
ENST00000262186.10:c.668C>T MANE Select	ENSP00000262186.5:p.Ala223Val
ENST00000262186.9:c.668C>T	ENSP00000262186.5:p.Ala223Val
ENST00000430723.4:c.320C>T	ENSP00000387657.4:p.Ala107Val
ENST00000532957.5:n.891C>T
NM_000238.3:c.668C>T , LRG_288t1:c.668C>T	NP_000229.1:p.Ala223Val
NM_172056.2:c.668C>T , LRG_288t2:c.668C>T	NP_742053.1:p.Ala223Val
XM_011516185.1:c.368C>T	XP_011514487.1:p.Ala123Val
XM_011516186.1:c.668C>T	XP_011514488.1:p.Ala223Val
XM_011516185.2:c.368C>T	XP_011514487.1:p.Ala123Val
XM_011516186.3:c.668C>T	XP_011514488.1:p.Ala223Val
XM_017012195.1:c.518C>T	XP_016867684.1:p.Ala173Val
XM_017012196.1:c.491C>T	XP_016867685.1:p.Ala164Val
NM_000238.4:c.668C>T MANE Select	NP_000229.1:p.Ala223Val