Canonical Allele Identifier: CA070885
Gene: KCNH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150648204G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951116G>A , CM000669.2:g.150951116G>A GRCh38
NC_000007.13:g.150648204G>A , CM000669.1:g.150648204G>A GRCh37
NC_000007.12:g.150279137G>A NCBI36
NG_008916.1:g.31811C>T , LRG_288:g.31811C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1248C>T
ENST00000683359.1:n.74C>T
ENST00000684241.1:n.2783C>T
ENST00000262186.10:c.1950C>T MANE Select ENSP00000262186.5:p.Leu650=
ENST00000330883.9:c.930C>T ENSP00000328531.4:p.Leu310=
ENST00000262186.9:c.1950C>T ENSP00000262186.5:p.Leu650=
ENST00000330883.8:c.930C>T ENSP00000328531.4:p.Leu310=
ENST00000430723.4:c.1602C>T ENSP00000387657.4:p.Leu534=
ENST00000461280.1:n.1237C>T
ENST00000473610.5:n.1582C>T
ENST00000532957.5:n.2173C>T
NM_000238.3:c.1950C>T , LRG_288t1:c.1950C>T NP_000229.1:p.Leu650=
NM_001204798.1:c.930C>T NP_001191727.1:p.Leu310=
NM_172056.2:c.1950C>T , LRG_288t2:c.1950C>T NP_742053.1:p.Leu650=
NM_172057.2:c.930C>T , LRG_288t3:c.930C>T NP_742054.1:p.Leu310=
XM_011516185.1:c.1650C>T XP_011514487.1:p.Leu550=
XM_011516186.1:c.1950C>T XP_011514488.1:p.Leu650=
XM_011516185.2:c.1650C>T XP_011514487.1:p.Leu550=
XM_011516186.3:c.1950C>T XP_011514488.1:p.Leu650=
XM_017012195.1:c.1800C>T XP_016867684.1:p.Leu600=
XM_017012196.1:c.1773C>T XP_016867685.1:p.Leu591=
NM_000238.4:c.1950C>T MANE Select NP_000229.1:p.Leu650=
NM_001204798.2:c.930C>T NP_001191727.1:p.Leu310=
NM_172057.3:c.930C>T NP_742054.1:p.Leu310=