Canonical Allele Identifier: CA369853696

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645561T>C (hg19) ; chr7:g.150948473T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948473T>C , CM000669.2:g.150948473T>C	GRCh38
NC_000007.13:g.150645561T>C , CM000669.1:g.150645561T>C	GRCh37
NC_000007.12:g.150276494T>C	NCBI36
NG_008916.1:g.34454A>G , LRG_288:g.34454A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3496A>G
ENST00000262186.10:c.2663A>G MANE Select	ENSP00000262186.5:p.Lys888Arg
ENST00000330883.9:c.1643A>G	ENSP00000328531.4:p.Lys548Arg
ENST00000262186.9:c.2663A>G	ENSP00000262186.5:p.Lys888Arg
ENST00000330883.8:c.1643A>G	ENSP00000328531.4:p.Lys548Arg
NM_000238.3:c.2663A>G , LRG_288t1:c.2663A>G	NP_000229.1:p.Lys888Arg
NM_172057.2:c.1643A>G , LRG_288t3:c.1643A>G	NP_742054.1:p.Lys548Arg
XM_011516185.1:c.2363A>G	XP_011514487.1:p.Lys788Arg
XM_011516186.1:c.2663A>G	XP_011514488.1:p.Lys888Arg
XM_011516185.2:c.2363A>G	XP_011514487.1:p.Lys788Arg
XM_011516186.3:c.2663A>G	XP_011514488.1:p.Lys888Arg
XM_017012195.1:c.2513A>G	XP_016867684.1:p.Lys838Arg
XM_017012196.1:c.2486A>G	XP_016867685.1:p.Lys829Arg
NM_000238.4:c.2663A>G MANE Select	NP_000229.1:p.Lys888Arg
NM_172057.3:c.1643A>G	NP_742054.1:p.Lys548Arg