Canonical Allele Identifier: CA369853938

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645623C>T (hg19) ; chr7:g.150948535C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948535C>T , CM000669.2:g.150948535C>T	GRCh38
NC_000007.13:g.150645623C>T , CM000669.1:g.150645623C>T	GRCh37
NC_000007.12:g.150276556C>T	NCBI36
NG_008916.1:g.34392G>A , LRG_288:g.34392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3434G>A
ENST00000262186.10:c.2601G>A MANE Select	ENSP00000262186.5:p.Met867Ile
ENST00000330883.9:c.1581G>A	ENSP00000328531.4:p.Met527Ile
ENST00000262186.9:c.2601G>A	ENSP00000262186.5:p.Met867Ile
ENST00000330883.8:c.1581G>A	ENSP00000328531.4:p.Met527Ile
NM_000238.3:c.2601G>A , LRG_288t1:c.2601G>A	NP_000229.1:p.Met867Ile
NM_172057.2:c.1581G>A , LRG_288t3:c.1581G>A	NP_742054.1:p.Met527Ile
XM_011516185.1:c.2301G>A	XP_011514487.1:p.Met767Ile
XM_011516186.1:c.2601G>A	XP_011514488.1:p.Met867Ile
XM_011516185.2:c.2301G>A	XP_011514487.1:p.Met767Ile
XM_011516186.3:c.2601G>A	XP_011514488.1:p.Met867Ile
XM_017012195.1:c.2451G>A	XP_016867684.1:p.Met817Ile
XM_017012196.1:c.2424G>A	XP_016867685.1:p.Met808Ile
NM_000238.4:c.2601G>A MANE Select	NP_000229.1:p.Met867Ile
NM_172057.3:c.1581G>A	NP_742054.1:p.Met527Ile