Canonical Allele Identifier: CA369857881

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 1359868
• ClinVar RCV Id: RCV001904585
• dbSNP Id: rs199472961
• MyVariant Identifiers: chr7:g.150648583T>G (hg19) ; chr7:g.150951495T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951495T>G , CM000669.2:g.150951495T>G	GRCh38
NC_000007.13:g.150648583T>G , CM000669.1:g.150648583T>G	GRCh37
NC_000007.12:g.150279516T>G	NCBI36
NG_008916.1:g.31432A>C , LRG_288:g.31432A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1196A>C
ENST00000683359.1:n.22A>C
ENST00000684241.1:n.2731A>C
ENST00000262186.10:c.1898A>C MANE Select	ENSP00000262186.5:p.Asn633Thr
ENST00000330883.9:c.878A>C	ENSP00000328531.4:p.Asn293Thr
ENST00000262186.9:c.1898A>C	ENSP00000262186.5:p.Asn633Thr
ENST00000330883.8:c.878A>C	ENSP00000328531.4:p.Asn293Thr
ENST00000430723.4:c.1550A>C	ENSP00000387657.4:p.Asn517Thr
ENST00000461280.1:n.1185A>C
ENST00000473610.5:n.1203A>C
ENST00000532957.5:n.2121A>C
NM_000238.3:c.1898A>C , LRG_288t1:c.1898A>C	NP_000229.1:p.Asn633Thr
NM_001204798.1:c.878A>C	NP_001191727.1:p.Asn293Thr
NM_172056.2:c.1898A>C , LRG_288t2:c.1898A>C	NP_742053.1:p.Asn633Thr
NM_172057.2:c.878A>C , LRG_288t3:c.878A>C	NP_742054.1:p.Asn293Thr
XM_011516185.1:c.1598A>C	XP_011514487.1:p.Asn533Thr
XM_011516186.1:c.1898A>C	XP_011514488.1:p.Asn633Thr
XM_011516185.2:c.1598A>C	XP_011514487.1:p.Asn533Thr
XM_011516186.3:c.1898A>C	XP_011514488.1:p.Asn633Thr
XM_017012195.1:c.1748A>C	XP_016867684.1:p.Asn583Thr
XM_017012196.1:c.1721A>C	XP_016867685.1:p.Asn574Thr
NM_000238.4:c.1898A>C MANE Select	NP_000229.1:p.Asn633Thr
NM_001204798.2:c.878A>C	NP_001191727.1:p.Asn293Thr
NM_172057.3:c.878A>C	NP_742054.1:p.Asn293Thr