Canonical Allele Identifier: CA006998

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948866T>C , CM000669.2:g.150948866T>C	GRCh38
NC_000007.13:g.150645954T>C , CM000669.1:g.150645954T>C	GRCh37
NC_000007.12:g.150276887T>C	NCBI36
NG_008916.1:g.34061A>G , LRG_288:g.34061A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000238.4:c.2582A>G MANE Select	NP_000229.1:p.Asn861Ser
ENST00000262186.10:c.2582A>G MANE Select	ENSP00000262186.5:p.Asn861Ser
NM_000238.3:c.2582A>G , LRG_288t1:c.2582A>G	NP_000229.1:p.Asn861Ser
NM_172057.2:c.1562A>G , LRG_288t3:c.1562A>G	NP_742054.1:p.Asn521Ser
NM_172057.3:c.1562A>G	NP_742054.1:p.Asn521Ser
ENST00000262186.9:c.2582A>G	ENSP00000262186.5:p.Asn861Ser
ENST00000330883.8:c.1562A>G	ENSP00000328531.4:p.Asn521Ser
ENST00000330883.9:c.1562A>G	ENSP00000328531.4:p.Asn521Ser
ENST00000684241.1:n.3415A>G
XM_011516185.1:c.2282A>G	XP_011514487.1:p.Asn761Ser
XM_011516185.2:c.2282A>G	XP_011514487.1:p.Asn761Ser
XM_011516186.1:c.2582A>G	XP_011514488.1:p.Asn861Ser
XM_011516186.3:c.2582A>G	XP_011514488.1:p.Asn861Ser
XM_017012195.1:c.2432A>G	XP_016867684.1:p.Asn811Ser
XM_017012196.1:c.2405A>G	XP_016867685.1:p.Asn802Ser