Canonical Allele Identifier: CA369860113

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649814A>G (hg19) ; chr7:g.150952726A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952726A>G , CM000669.2:g.150952726A>G	GRCh38
NC_000007.13:g.150649814A>G , CM000669.1:g.150649814A>G	GRCh37
NC_000007.12:g.150280747A>G	NCBI36
NG_008916.1:g.30201T>C , LRG_288:g.30201T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.554T>C
ENST00000684116.1:n.149T>C
ENST00000684241.1:n.2089T>C
ENST00000262186.10:c.1256T>C MANE Select	ENSP00000262186.5:p.Ile419Thr
ENST00000330883.9:c.236T>C	ENSP00000328531.4:p.Ile79Thr
ENST00000262186.9:c.1256T>C	ENSP00000262186.5:p.Ile419Thr
ENST00000330883.8:c.236T>C	ENSP00000328531.4:p.Ile79Thr
ENST00000430723.4:c.908T>C	ENSP00000387657.4:p.Ile303Thr
ENST00000461280.1:n.543T>C
ENST00000473610.5:n.561T>C
ENST00000532957.5:n.1479T>C
NM_000238.3:c.1256T>C , LRG_288t1:c.1256T>C	NP_000229.1:p.Ile419Thr
NM_001204798.1:c.236T>C	NP_001191727.1:p.Ile79Thr
NM_172056.2:c.1256T>C , LRG_288t2:c.1256T>C	NP_742053.1:p.Ile419Thr
NM_172057.2:c.236T>C , LRG_288t3:c.236T>C	NP_742054.1:p.Ile79Thr
XM_011516185.1:c.956T>C	XP_011514487.1:p.Ile319Thr
XM_011516186.1:c.1256T>C	XP_011514488.1:p.Ile419Thr
XM_011516185.2:c.956T>C	XP_011514487.1:p.Ile319Thr
XM_011516186.3:c.1256T>C	XP_011514488.1:p.Ile419Thr
XM_017012195.1:c.1106T>C	XP_016867684.1:p.Ile369Thr
XM_017012196.1:c.1079T>C	XP_016867685.1:p.Ile360Thr
NM_000238.4:c.1256T>C MANE Select	NP_000229.1:p.Ile419Thr
NM_001204798.2:c.236T>C	NP_001191727.1:p.Ile79Thr
NM_172057.3:c.236T>C	NP_742054.1:p.Ile79Thr