Canonical Allele Identifier: CA369856645

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647474T>C (hg19) ; chr7:g.150950386T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950386T>C , CM000669.2:g.150950386T>C	GRCh38
NC_000007.13:g.150647474T>C , CM000669.1:g.150647474T>C	GRCh37
NC_000007.12:g.150278407T>C	NCBI36
NG_008916.1:g.32541A>G , LRG_288:g.32541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1478A>G
ENST00000684241.1:n.3013A>G
ENST00000262186.10:c.2180A>G MANE Select	ENSP00000262186.5:p.Asp727Gly
ENST00000330883.9:c.1160A>G	ENSP00000328531.4:p.Asp387Gly
ENST00000262186.9:c.2180A>G	ENSP00000262186.5:p.Asp727Gly
ENST00000330883.8:c.1160A>G	ENSP00000328531.4:p.Asp387Gly
ENST00000430723.4:c.1832A>G	ENSP00000387657.4:p.Asp611Gly
ENST00000461280.1:n.1467A>G
ENST00000473610.5:n.1812A>G
ENST00000532957.5:n.2403A>G
NM_000238.3:c.2180A>G , LRG_288t1:c.2180A>G	NP_000229.1:p.Asp727Gly
NM_001204798.1:c.1160A>G	NP_001191727.1:p.Asp387Gly
NM_172056.2:c.2180A>G , LRG_288t2:c.2180A>G	NP_742053.1:p.Asp727Gly
NM_172057.2:c.1160A>G , LRG_288t3:c.1160A>G	NP_742054.1:p.Asp387Gly
XM_011516185.1:c.1880A>G	XP_011514487.1:p.Asp627Gly
XM_011516186.1:c.2180A>G	XP_011514488.1:p.Asp727Gly
XM_011516185.2:c.1880A>G	XP_011514487.1:p.Asp627Gly
XM_011516186.3:c.2180A>G	XP_011514488.1:p.Asp727Gly
XM_017012195.1:c.2030A>G	XP_016867684.1:p.Asp677Gly
XM_017012196.1:c.2003A>G	XP_016867685.1:p.Asp668Gly
NM_000238.4:c.2180A>G MANE Select	NP_000229.1:p.Asp727Gly
NM_001204798.2:c.1160A>G	NP_001191727.1:p.Asp387Gly
NM_172057.3:c.1160A>G	NP_742054.1:p.Asp387Gly