Canonical Allele Identifier: CA369851613

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150642593A>C (hg19) ; chr7:g.150945505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150945505A>C , CM000669.2:g.150945505A>C	GRCh38
NC_000007.13:g.150642593A>C , CM000669.1:g.150642593A>C	GRCh37
NC_000007.12:g.150273526A>C	NCBI36
NG_008916.1:g.37422T>G , LRG_288:g.37422T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.4173T>G
ENST00000262186.10:c.3340T>G MANE Select	ENSP00000262186.5:p.Phe1114Val
ENST00000330883.9:c.2320T>G	ENSP00000328531.4:p.Phe774Val
ENST00000262186.9:c.3340T>G	ENSP00000262186.5:p.Phe1114Val
ENST00000330883.8:c.2320T>G	ENSP00000328531.4:p.Phe774Val
NM_000238.3:c.3340T>G , LRG_288t1:c.3340T>G	NP_000229.1:p.Phe1114Val
NM_172057.2:c.2320T>G , LRG_288t3:c.2320T>G	NP_742054.1:p.Phe774Val
XM_011516185.1:c.3040T>G	XP_011514487.1:p.Phe1014Val
XM_011516185.2:c.3040T>G	XP_011514487.1:p.Phe1014Val
XM_017012195.1:c.3190T>G	XP_016867684.1:p.Phe1064Val
XM_017012196.1:c.3163T>G	XP_016867685.1:p.Phe1055Val
NM_000238.4:c.3340T>G MANE Select	NP_000229.1:p.Phe1114Val
NM_172057.3:c.2320T>G	NP_742054.1:p.Phe774Val