Canonical Allele Identifier: CA369863530

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958479-T-C
• MyVariant Identifiers: chr7:g.150655567T>C (hg19) ; chr7:g.150958479T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958479T>C , CM000669.2:g.150958479T>C	GRCh38
NC_000007.13:g.150655567T>C , CM000669.1:g.150655567T>C	GRCh37
NC_000007.12:g.150286500T>C	NCBI36
NG_008916.1:g.24448A>G , LRG_288:g.24448A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1329A>G
ENST00000262186.10:c.496A>G MANE Select	ENSP00000262186.5:p.Lys166Glu
ENST00000262186.9:c.496A>G	ENSP00000262186.5:p.Lys166Glu
ENST00000430723.4:c.235-87A>G	ENSP00000387657.4:n.235-87A>G
ENST00000532957.5:n.719A>G
NM_000238.3:c.496A>G , LRG_288t1:c.496A>G	NP_000229.1:p.Lys166Glu
NM_172056.2:c.496A>G , LRG_288t2:c.496A>G	NP_742053.1:p.Lys166Glu
XM_011516185.1:c.196A>G	XP_011514487.1:p.Lys66Glu
XM_011516186.1:c.496A>G	XP_011514488.1:p.Lys166Glu
XM_011516185.2:c.196A>G	XP_011514487.1:p.Lys66Glu
XM_011516186.3:c.496A>G	XP_011514488.1:p.Lys166Glu
XM_017012195.1:c.346A>G	XP_016867684.1:p.Lys116Glu
XM_017012196.1:c.319A>G	XP_016867685.1:p.Lys107Glu
NM_000238.4:c.496A>G MANE Select	NP_000229.1:p.Lys166Glu