Canonical Allele Identifier: CA369857396

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648040C>G (hg19) ; chr7:g.150950952C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950952C>G , CM000669.2:g.150950952C>G	GRCh38
NC_000007.13:g.150648040C>G , CM000669.1:g.150648040C>G	GRCh37
NC_000007.12:g.150278973C>G	NCBI36
NG_008916.1:g.31975G>C , LRG_288:g.31975G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1412G>C
ENST00000683359.1:n.238G>C
ENST00000684241.1:n.2947G>C
ENST00000262186.10:c.2114G>C MANE Select	ENSP00000262186.5:p.Trp705Ser
ENST00000330883.9:c.1094G>C	ENSP00000328531.4:p.Trp365Ser
ENST00000262186.9:c.2114G>C	ENSP00000262186.5:p.Trp705Ser
ENST00000330883.8:c.1094G>C	ENSP00000328531.4:p.Trp365Ser
ENST00000430723.4:c.1766G>C	ENSP00000387657.4:p.Trp589Ser
ENST00000461280.1:n.1401G>C
ENST00000473610.5:n.1746G>C
ENST00000532957.5:n.2337G>C
NM_000238.3:c.2114G>C , LRG_288t1:c.2114G>C	NP_000229.1:p.Trp705Ser
NM_001204798.1:c.1094G>C	NP_001191727.1:p.Trp365Ser
NM_172056.2:c.2114G>C , LRG_288t2:c.2114G>C	NP_742053.1:p.Trp705Ser
NM_172057.2:c.1094G>C , LRG_288t3:c.1094G>C	NP_742054.1:p.Trp365Ser
XM_011516185.1:c.1814G>C	XP_011514487.1:p.Trp605Ser
XM_011516186.1:c.2114G>C	XP_011514488.1:p.Trp705Ser
XM_011516185.2:c.1814G>C	XP_011514487.1:p.Trp605Ser
XM_011516186.3:c.2114G>C	XP_011514488.1:p.Trp705Ser
XM_017012195.1:c.1964G>C	XP_016867684.1:p.Trp655Ser
XM_017012196.1:c.1937G>C	XP_016867685.1:p.Trp646Ser
NM_000238.4:c.2114G>C MANE Select	NP_000229.1:p.Trp705Ser
NM_001204798.2:c.1094G>C	NP_001191727.1:p.Trp365Ser
NM_172057.3:c.1094G>C	NP_742054.1:p.Trp365Ser