Canonical Allele Identifier: CA458871380

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647428G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950340G>T , CM000669.2:g.150950340G>T	GRCh38
NC_000007.13:g.150647428G>T , CM000669.1:g.150647428G>T	GRCh37
NC_000007.12:g.150278361G>T	NCBI36
NG_008916.1:g.32587C>A , LRG_288:g.32587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1524C>A
ENST00000684241.1:n.3059C>A
ENST00000262186.10:c.2226C>A MANE Select	ENSP00000262186.5:p.Pro742=
ENST00000330883.9:c.1206C>A	ENSP00000328531.4:p.Pro402=
ENST00000262186.9:c.2226C>A	ENSP00000262186.5:p.Pro742=
ENST00000330883.8:c.1206C>A	ENSP00000328531.4:p.Pro402=
ENST00000430723.4:c.1878C>A	ENSP00000387657.4:p.Pro626=
ENST00000461280.1:n.1513C>A
ENST00000473610.5:n.1858C>A
ENST00000532957.5:n.2449C>A
NM_000238.3:c.2226C>A , LRG_288t1:c.2226C>A	NP_000229.1:p.Pro742=
NM_001204798.1:c.1206C>A	NP_001191727.1:p.Pro402=
NM_172056.2:c.2226C>A , LRG_288t2:c.2226C>A	NP_742053.1:p.Pro742=
NM_172057.2:c.1206C>A , LRG_288t3:c.1206C>A	NP_742054.1:p.Pro402=
XM_011516185.1:c.1926C>A	XP_011514487.1:p.Pro642=
XM_011516186.1:c.2226C>A	XP_011514488.1:p.Pro742=
XM_011516185.2:c.1926C>A	XP_011514487.1:p.Pro642=
XM_011516186.3:c.2226C>A	XP_011514488.1:p.Pro742=
XM_017012195.1:c.2076C>A	XP_016867684.1:p.Pro692=
XM_017012196.1:c.2049C>A	XP_016867685.1:p.Pro683=
NM_000238.4:c.2226C>A MANE Select	NP_000229.1:p.Pro742=
NM_001204798.2:c.1206C>A	NP_001191727.1:p.Pro402=
NM_172057.3:c.1206C>A	NP_742054.1:p.Pro402=