Canonical Allele Identifier: CA369862046

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958062-T-C
• MyVariant Identifiers: chr7:g.150655150T>C (hg19) ; chr7:g.150958062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958062T>C , CM000669.2:g.150958062T>C	GRCh38
NC_000007.13:g.150655150T>C , CM000669.1:g.150655150T>C	GRCh37
NC_000007.12:g.150286083T>C	NCBI36
NG_008916.1:g.24865A>G , LRG_288:g.24865A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1746A>G
ENST00000262186.10:c.913A>G MANE Select	ENSP00000262186.5:p.Thr305Ala
ENST00000262186.9:c.913A>G	ENSP00000262186.5:p.Thr305Ala
ENST00000430723.4:c.565A>G	ENSP00000387657.4:p.Thr189Ala
ENST00000532957.5:n.1136A>G
NM_000238.3:c.913A>G , LRG_288t1:c.913A>G	NP_000229.1:p.Thr305Ala
NM_172056.2:c.913A>G , LRG_288t2:c.913A>G	NP_742053.1:p.Thr305Ala
XM_011516185.1:c.613A>G	XP_011514487.1:p.Thr205Ala
XM_011516186.1:c.913A>G	XP_011514488.1:p.Thr305Ala
XM_011516185.2:c.613A>G	XP_011514487.1:p.Thr205Ala
XM_011516186.3:c.913A>G	XP_011514488.1:p.Thr305Ala
XM_017012195.1:c.763A>G	XP_016867684.1:p.Thr255Ala
XM_017012196.1:c.736A>G	XP_016867685.1:p.Thr246Ala
NM_000238.4:c.913A>G MANE Select	NP_000229.1:p.Thr305Ala