Canonical Allele Identifier: CA369856620

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647468C>G (hg19) ; chr7:g.150950380C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950380C>G , CM000669.2:g.150950380C>G	GRCh38
NC_000007.13:g.150647468C>G , CM000669.1:g.150647468C>G	GRCh37
NC_000007.12:g.150278401C>G	NCBI36
NG_008916.1:g.32547G>C , LRG_288:g.32547G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1484G>C
ENST00000684241.1:n.3019G>C
ENST00000262186.10:c.2186G>C MANE Select	ENSP00000262186.5:p.Cys729Ser
ENST00000330883.9:c.1166G>C	ENSP00000328531.4:p.Cys389Ser
ENST00000262186.9:c.2186G>C	ENSP00000262186.5:p.Cys729Ser
ENST00000330883.8:c.1166G>C	ENSP00000328531.4:p.Cys389Ser
ENST00000430723.4:c.1838G>C	ENSP00000387657.4:p.Cys613Ser
ENST00000461280.1:n.1473G>C
ENST00000473610.5:n.1818G>C
ENST00000532957.5:n.2409G>C
NM_000238.3:c.2186G>C , LRG_288t1:c.2186G>C	NP_000229.1:p.Cys729Ser
NM_001204798.1:c.1166G>C	NP_001191727.1:p.Cys389Ser
NM_172056.2:c.2186G>C , LRG_288t2:c.2186G>C	NP_742053.1:p.Cys729Ser
NM_172057.2:c.1166G>C , LRG_288t3:c.1166G>C	NP_742054.1:p.Cys389Ser
XM_011516185.1:c.1886G>C	XP_011514487.1:p.Cys629Ser
XM_011516186.1:c.2186G>C	XP_011514488.1:p.Cys729Ser
XM_011516185.2:c.1886G>C	XP_011514487.1:p.Cys629Ser
XM_011516186.3:c.2186G>C	XP_011514488.1:p.Cys729Ser
XM_017012195.1:c.2036G>C	XP_016867684.1:p.Cys679Ser
XM_017012196.1:c.2009G>C	XP_016867685.1:p.Cys670Ser
NM_000238.4:c.2186G>C MANE Select	NP_000229.1:p.Cys729Ser
NM_001204798.2:c.1166G>C	NP_001191727.1:p.Cys389Ser
NM_172057.3:c.1166G>C	NP_742054.1:p.Cys389Ser