Canonical Allele Identifier: CA458871459

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648564G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951476G>A , CM000669.2:g.150951476G>A	GRCh38
NC_000007.13:g.150648564G>A , CM000669.1:g.150648564G>A	GRCh37
NC_000007.12:g.150279497G>A	NCBI36
NG_008916.1:g.31451C>T , LRG_288:g.31451C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1215C>T
ENST00000683359.1:n.41C>T
ENST00000684241.1:n.2750C>T
ENST00000262186.10:c.1917C>T MANE Select	ENSP00000262186.5:p.Ile639=
ENST00000330883.9:c.897C>T	ENSP00000328531.4:p.Ile299=
ENST00000262186.9:c.1917C>T	ENSP00000262186.5:p.Ile639=
ENST00000330883.8:c.897C>T	ENSP00000328531.4:p.Ile299=
ENST00000430723.4:c.1569C>T	ENSP00000387657.4:p.Ile523=
ENST00000461280.1:n.1204C>T
ENST00000473610.5:n.1222C>T
ENST00000532957.5:n.2140C>T
NM_000238.3:c.1917C>T , LRG_288t1:c.1917C>T	NP_000229.1:p.Ile639=
NM_001204798.1:c.897C>T	NP_001191727.1:p.Ile299=
NM_172056.2:c.1917C>T , LRG_288t2:c.1917C>T	NP_742053.1:p.Ile639=
NM_172057.2:c.897C>T , LRG_288t3:c.897C>T	NP_742054.1:p.Ile299=
XM_011516185.1:c.1617C>T	XP_011514487.1:p.Ile539=
XM_011516186.1:c.1917C>T	XP_011514488.1:p.Ile639=
XM_011516185.2:c.1617C>T	XP_011514487.1:p.Ile539=
XM_011516186.3:c.1917C>T	XP_011514488.1:p.Ile639=
XM_017012195.1:c.1767C>T	XP_016867684.1:p.Ile589=
XM_017012196.1:c.1740C>T	XP_016867685.1:p.Ile580=
NM_000238.4:c.1917C>T MANE Select	NP_000229.1:p.Ile639=
NM_001204798.2:c.897C>T	NP_001191727.1:p.Ile299=
NM_172057.3:c.897C>T	NP_742054.1:p.Ile299=