Canonical Allele Identifier: CA369858139

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648733A>T (hg19) ; chr7:g.150951645A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951645A>T , CM000669.2:g.150951645A>T	GRCh38
NC_000007.13:g.150648733A>T , CM000669.1:g.150648733A>T	GRCh37
NC_000007.12:g.150279666A>T	NCBI36
NG_008916.1:g.31282T>A , LRG_288:g.31282T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1046T>A
ENST00000684241.1:n.2581T>A
ENST00000262186.10:c.1748T>A MANE Select	ENSP00000262186.5:p.Ile583Asn
ENST00000330883.9:c.728T>A	ENSP00000328531.4:p.Ile243Asn
ENST00000262186.9:c.1748T>A	ENSP00000262186.5:p.Ile583Asn
ENST00000330883.8:c.728T>A	ENSP00000328531.4:p.Ile243Asn
ENST00000430723.4:c.1400T>A	ENSP00000387657.4:p.Ile467Asn
ENST00000461280.1:n.1035T>A
ENST00000473610.5:n.1053T>A
ENST00000532957.5:n.1971T>A
NM_000238.3:c.1748T>A , LRG_288t1:c.1748T>A	NP_000229.1:p.Ile583Asn
NM_001204798.1:c.728T>A	NP_001191727.1:p.Ile243Asn
NM_172056.2:c.1748T>A , LRG_288t2:c.1748T>A	NP_742053.1:p.Ile583Asn
NM_172057.2:c.728T>A , LRG_288t3:c.728T>A	NP_742054.1:p.Ile243Asn
XM_011516185.1:c.1448T>A	XP_011514487.1:p.Ile483Asn
XM_011516186.1:c.1748T>A	XP_011514488.1:p.Ile583Asn
XM_011516185.2:c.1448T>A	XP_011514487.1:p.Ile483Asn
XM_011516186.3:c.1748T>A	XP_011514488.1:p.Ile583Asn
XM_017012195.1:c.1598T>A	XP_016867684.1:p.Ile533Asn
XM_017012196.1:c.1571T>A	XP_016867685.1:p.Ile524Asn
NM_000238.4:c.1748T>A MANE Select	NP_000229.1:p.Ile583Asn
NM_001204798.2:c.728T>A	NP_001191727.1:p.Ile243Asn
NM_172057.3:c.728T>A	NP_742054.1:p.Ile243Asn