Canonical Allele Identifier: CA369862457

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655267T>G (hg19) ; chr7:g.150958179T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958179T>G , CM000669.2:g.150958179T>G	GRCh38
NC_000007.13:g.150655267T>G , CM000669.1:g.150655267T>G	GRCh37
NC_000007.12:g.150286200T>G	NCBI36
NG_008916.1:g.24748A>C , LRG_288:g.24748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1629A>C
ENST00000262186.10:c.796A>C MANE Select	ENSP00000262186.5:p.Ser266Arg
ENST00000262186.9:c.796A>C	ENSP00000262186.5:p.Ser266Arg
ENST00000430723.4:c.448A>C	ENSP00000387657.4:p.Ser150Arg
ENST00000532957.5:n.1019A>C
NM_000238.3:c.796A>C , LRG_288t1:c.796A>C	NP_000229.1:p.Ser266Arg
NM_172056.2:c.796A>C , LRG_288t2:c.796A>C	NP_742053.1:p.Ser266Arg
XM_011516185.1:c.496A>C	XP_011514487.1:p.Ser166Arg
XM_011516186.1:c.796A>C	XP_011514488.1:p.Ser266Arg
XM_011516185.2:c.496A>C	XP_011514487.1:p.Ser166Arg
XM_011516186.3:c.796A>C	XP_011514488.1:p.Ser266Arg
XM_017012195.1:c.646A>C	XP_016867684.1:p.Ser216Arg
XM_017012196.1:c.619A>C	XP_016867685.1:p.Ser207Arg
NM_000238.4:c.796A>C MANE Select	NP_000229.1:p.Ser266Arg