Canonical Allele Identifier: CA369860189

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649851T>G (hg19) ; chr7:g.150952763T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952763T>G , CM000669.2:g.150952763T>G	GRCh38
NC_000007.13:g.150649851T>G , CM000669.1:g.150649851T>G	GRCh37
NC_000007.12:g.150280784T>G	NCBI36
NG_008916.1:g.30164A>C , LRG_288:g.30164A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.517A>C
ENST00000684116.1:n.112A>C
ENST00000684241.1:n.2052A>C
ENST00000262186.10:c.1219A>C MANE Select	ENSP00000262186.5:p.Lys407Gln
ENST00000330883.9:c.199A>C	ENSP00000328531.4:p.Lys67Gln
ENST00000262186.9:c.1219A>C	ENSP00000262186.5:p.Lys407Gln
ENST00000330883.8:c.199A>C	ENSP00000328531.4:p.Lys67Gln
ENST00000430723.4:c.871A>C	ENSP00000387657.4:p.Lys291Gln
ENST00000461280.1:n.506A>C
ENST00000473610.5:n.524A>C
ENST00000532957.5:n.1442A>C
NM_000238.3:c.1219A>C , LRG_288t1:c.1219A>C	NP_000229.1:p.Lys407Gln
NM_001204798.1:c.199A>C	NP_001191727.1:p.Lys67Gln
NM_172056.2:c.1219A>C , LRG_288t2:c.1219A>C	NP_742053.1:p.Lys407Gln
NM_172057.2:c.199A>C , LRG_288t3:c.199A>C	NP_742054.1:p.Lys67Gln
XM_011516185.1:c.919A>C	XP_011514487.1:p.Lys307Gln
XM_011516186.1:c.1219A>C	XP_011514488.1:p.Lys407Gln
XM_011516185.2:c.919A>C	XP_011514487.1:p.Lys307Gln
XM_011516186.3:c.1219A>C	XP_011514488.1:p.Lys407Gln
XM_017012195.1:c.1069A>C	XP_016867684.1:p.Lys357Gln
XM_017012196.1:c.1042A>C	XP_016867685.1:p.Lys348Gln
NM_000238.4:c.1219A>C MANE Select	NP_000229.1:p.Lys407Gln
NM_001204798.2:c.199A>C	NP_001191727.1:p.Lys67Gln
NM_172057.3:c.199A>C	NP_742054.1:p.Lys67Gln