Canonical Allele Identifier: CA369858065

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648691T>A (hg19) ; chr7:g.150951603T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951603T>A , CM000669.2:g.150951603T>A	GRCh38
NC_000007.13:g.150648691T>A , CM000669.1:g.150648691T>A	GRCh37
NC_000007.12:g.150279624T>A	NCBI36
NG_008916.1:g.31324A>T , LRG_288:g.31324A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1088A>T
ENST00000684241.1:n.2623A>T
ENST00000262186.10:c.1790A>T MANE Select	ENSP00000262186.5:p.Tyr597Phe
ENST00000330883.9:c.770A>T	ENSP00000328531.4:p.Tyr257Phe
ENST00000262186.9:c.1790A>T	ENSP00000262186.5:p.Tyr597Phe
ENST00000330883.8:c.770A>T	ENSP00000328531.4:p.Tyr257Phe
ENST00000430723.4:c.1442A>T	ENSP00000387657.4:p.Tyr481Phe
ENST00000461280.1:n.1077A>T
ENST00000473610.5:n.1095A>T
ENST00000532957.5:n.2013A>T
NM_000238.3:c.1790A>T , LRG_288t1:c.1790A>T	NP_000229.1:p.Tyr597Phe
NM_001204798.1:c.770A>T	NP_001191727.1:p.Tyr257Phe
NM_172056.2:c.1790A>T , LRG_288t2:c.1790A>T	NP_742053.1:p.Tyr597Phe
NM_172057.2:c.770A>T , LRG_288t3:c.770A>T	NP_742054.1:p.Tyr257Phe
XM_011516185.1:c.1490A>T	XP_011514487.1:p.Tyr497Phe
XM_011516186.1:c.1790A>T	XP_011514488.1:p.Tyr597Phe
XM_011516185.2:c.1490A>T	XP_011514487.1:p.Tyr497Phe
XM_011516186.3:c.1790A>T	XP_011514488.1:p.Tyr597Phe
XM_017012195.1:c.1640A>T	XP_016867684.1:p.Tyr547Phe
XM_017012196.1:c.1613A>T	XP_016867685.1:p.Tyr538Phe
NM_000238.4:c.1790A>T MANE Select	NP_000229.1:p.Tyr597Phe
NM_001204798.2:c.770A>T	NP_001191727.1:p.Tyr257Phe
NM_172057.3:c.770A>T	NP_742054.1:p.Tyr257Phe