Canonical Allele Identifier: CA369857769

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648199T>C (hg19) ; chr7:g.150951111T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951111T>C , CM000669.2:g.150951111T>C	GRCh38
NC_000007.13:g.150648199T>C , CM000669.1:g.150648199T>C	GRCh37
NC_000007.12:g.150279132T>C	NCBI36
NG_008916.1:g.31816A>G , LRG_288:g.31816A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1253A>G
ENST00000683359.1:n.79A>G
ENST00000684241.1:n.2788A>G
ENST00000262186.10:c.1955A>G MANE Select	ENSP00000262186.5:p.Tyr652Cys
ENST00000330883.9:c.935A>G	ENSP00000328531.4:p.Tyr312Cys
ENST00000262186.9:c.1955A>G	ENSP00000262186.5:p.Tyr652Cys
ENST00000330883.8:c.935A>G	ENSP00000328531.4:p.Tyr312Cys
ENST00000430723.4:c.1607A>G	ENSP00000387657.4:p.Tyr536Cys
ENST00000461280.1:n.1242A>G
ENST00000473610.5:n.1587A>G
ENST00000532957.5:n.2178A>G
NM_000238.3:c.1955A>G , LRG_288t1:c.1955A>G	NP_000229.1:p.Tyr652Cys
NM_001204798.1:c.935A>G	NP_001191727.1:p.Tyr312Cys
NM_172056.2:c.1955A>G , LRG_288t2:c.1955A>G	NP_742053.1:p.Tyr652Cys
NM_172057.2:c.935A>G , LRG_288t3:c.935A>G	NP_742054.1:p.Tyr312Cys
XM_011516185.1:c.1655A>G	XP_011514487.1:p.Tyr552Cys
XM_011516186.1:c.1955A>G	XP_011514488.1:p.Tyr652Cys
XM_011516185.2:c.1655A>G	XP_011514487.1:p.Tyr552Cys
XM_011516186.3:c.1955A>G	XP_011514488.1:p.Tyr652Cys
XM_017012195.1:c.1805A>G	XP_016867684.1:p.Tyr602Cys
XM_017012196.1:c.1778A>G	XP_016867685.1:p.Tyr593Cys
NM_000238.4:c.1955A>G MANE Select	NP_000229.1:p.Tyr652Cys
NM_001204798.2:c.935A>G	NP_001191727.1:p.Tyr312Cys
NM_172057.3:c.935A>G	NP_742054.1:p.Tyr312Cys