Canonical Allele Identifier: CA369858163

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648746T>A (hg19) ; chr7:g.150951658T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951658T>A , CM000669.2:g.150951658T>A	GRCh38
NC_000007.13:g.150648746T>A , CM000669.1:g.150648746T>A	GRCh37
NC_000007.12:g.150279679T>A	NCBI36
NG_008916.1:g.31269A>T , LRG_288:g.31269A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1033A>T
ENST00000684241.1:n.2568A>T
ENST00000262186.10:c.1735A>T MANE Select	ENSP00000262186.5:p.Met579Leu
ENST00000330883.9:c.715A>T	ENSP00000328531.4:p.Met239Leu
ENST00000262186.9:c.1735A>T	ENSP00000262186.5:p.Met579Leu
ENST00000330883.8:c.715A>T	ENSP00000328531.4:p.Met239Leu
ENST00000430723.4:c.1387A>T	ENSP00000387657.4:p.Met463Leu
ENST00000461280.1:n.1022A>T
ENST00000473610.5:n.1040A>T
ENST00000532957.5:n.1958A>T
NM_000238.3:c.1735A>T , LRG_288t1:c.1735A>T	NP_000229.1:p.Met579Leu
NM_001204798.1:c.715A>T	NP_001191727.1:p.Met239Leu
NM_172056.2:c.1735A>T , LRG_288t2:c.1735A>T	NP_742053.1:p.Met579Leu
NM_172057.2:c.715A>T , LRG_288t3:c.715A>T	NP_742054.1:p.Met239Leu
XM_011516185.1:c.1435A>T	XP_011514487.1:p.Met479Leu
XM_011516186.1:c.1735A>T	XP_011514488.1:p.Met579Leu
XM_011516185.2:c.1435A>T	XP_011514487.1:p.Met479Leu
XM_011516186.3:c.1735A>T	XP_011514488.1:p.Met579Leu
XM_017012195.1:c.1585A>T	XP_016867684.1:p.Met529Leu
XM_017012196.1:c.1558A>T	XP_016867685.1:p.Met520Leu
NM_000238.4:c.1735A>T MANE Select	NP_000229.1:p.Met579Leu
NM_001204798.2:c.715A>T	NP_001191727.1:p.Met239Leu
NM_172057.3:c.715A>T	NP_742054.1:p.Met239Leu