Canonical Allele Identifier: CA369863031

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958341-G-T
• MyVariant Identifiers: chr7:g.150655429G>T (hg19) ; chr7:g.150958341G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958341G>T , CM000669.2:g.150958341G>T	GRCh38
NC_000007.13:g.150655429G>T , CM000669.1:g.150655429G>T	GRCh37
NC_000007.12:g.150286362G>T	NCBI36
NG_008916.1:g.24586C>A , LRG_288:g.24586C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1467C>A
ENST00000262186.10:c.634C>A MANE Select	ENSP00000262186.5:p.Leu212Met
ENST00000262186.9:c.634C>A	ENSP00000262186.5:p.Leu212Met
ENST00000430723.4:c.286C>A	ENSP00000387657.4:p.Leu96Met
ENST00000532957.5:n.857C>A
NM_000238.3:c.634C>A , LRG_288t1:c.634C>A	NP_000229.1:p.Leu212Met
NM_172056.2:c.634C>A , LRG_288t2:c.634C>A	NP_742053.1:p.Leu212Met
XM_011516185.1:c.334C>A	XP_011514487.1:p.Leu112Met
XM_011516186.1:c.634C>A	XP_011514488.1:p.Leu212Met
XM_011516185.2:c.334C>A	XP_011514487.1:p.Leu112Met
XM_011516186.3:c.634C>A	XP_011514488.1:p.Leu212Met
XM_017012195.1:c.484C>A	XP_016867684.1:p.Leu162Met
XM_017012196.1:c.457C>A	XP_016867685.1:p.Leu153Met
NM_000238.4:c.634C>A MANE Select	NP_000229.1:p.Leu212Met