Canonical Allele Identifier: CA369861893

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150957481-C-T
• MyVariant Identifiers: chr7:g.150654569C>T (hg19) ; chr7:g.150957481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957481C>T , CM000669.2:g.150957481C>T	GRCh38
NC_000007.13:g.150654569C>T , CM000669.1:g.150654569C>T	GRCh37
NC_000007.12:g.150285502C>T	NCBI36
NG_008916.1:g.25446G>A , LRG_288:g.25446G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1771G>A
ENST00000262186.10:c.938G>A MANE Select	ENSP00000262186.5:p.Ser313Asn
ENST00000262186.9:c.938G>A	ENSP00000262186.5:p.Ser313Asn
ENST00000430723.4:c.590G>A	ENSP00000387657.4:p.Ser197Asn
ENST00000532957.5:n.1161G>A
NM_000238.3:c.938G>A , LRG_288t1:c.938G>A	NP_000229.1:p.Ser313Asn
NM_172056.2:c.938G>A , LRG_288t2:c.938G>A	NP_742053.1:p.Ser313Asn
XM_011516185.1:c.638G>A	XP_011514487.1:p.Ser213Asn
XM_011516186.1:c.938G>A	XP_011514488.1:p.Ser313Asn
XM_011516185.2:c.638G>A	XP_011514487.1:p.Ser213Asn
XM_011516186.3:c.938G>A	XP_011514488.1:p.Ser313Asn
XM_017012195.1:c.788G>A	XP_016867684.1:p.Ser263Asn
XM_017012196.1:c.761G>A	XP_016867685.1:p.Ser254Asn
NM_000238.4:c.938G>A MANE Select	NP_000229.1:p.Ser313Asn