Canonical Allele Identifier: CA071886

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958289-T-C
• MyVariant Identifiers: chr7:g.150655377T>C (hg19) ; chr7:g.150958289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958289T>C , CM000669.2:g.150958289T>C	GRCh38
NC_000007.13:g.150655377T>C , CM000669.1:g.150655377T>C	GRCh37
NC_000007.12:g.150286310T>C	NCBI36
NG_008916.1:g.24638A>G , LRG_288:g.24638A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1519A>G
ENST00000262186.10:c.686A>G MANE Select	ENSP00000262186.5:p.Glu229Gly
ENST00000262186.9:c.686A>G	ENSP00000262186.5:p.Glu229Gly
ENST00000430723.4:c.338A>G	ENSP00000387657.4:p.Glu113Gly
ENST00000532957.5:n.909A>G
NM_000238.3:c.686A>G , LRG_288t1:c.686A>G	NP_000229.1:p.Glu229Gly
NM_172056.2:c.686A>G , LRG_288t2:c.686A>G	NP_742053.1:p.Glu229Gly
XM_011516185.1:c.386A>G	XP_011514487.1:p.Glu129Gly
XM_011516186.1:c.686A>G	XP_011514488.1:p.Glu229Gly
XM_011516185.2:c.386A>G	XP_011514487.1:p.Glu129Gly
XM_011516186.3:c.686A>G	XP_011514488.1:p.Glu229Gly
XM_017012195.1:c.536A>G	XP_016867684.1:p.Glu179Gly
XM_017012196.1:c.509A>G	XP_016867685.1:p.Glu170Gly
NM_000238.4:c.686A>G MANE Select	NP_000229.1:p.Glu229Gly