Canonical Allele Identifier: CA369863813

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656767A>T (hg19) ; chr7:g.150959679A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959679A>T , CM000669.2:g.150959679A>T	GRCh38
NC_000007.13:g.150656767A>T , CM000669.1:g.150656767A>T	GRCh37
NC_000007.12:g.150287700A>T	NCBI36
NG_008916.1:g.23248T>A , LRG_288:g.23248T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1198T>A
ENST00000262186.10:c.365T>A MANE Select	ENSP00000262186.5:p.Val122Asp
ENST00000262186.9:c.365T>A	ENSP00000262186.5:p.Val122Asp
ENST00000430723.4:c.188T>A	ENSP00000387657.4:p.Val63Asp
ENST00000532957.5:n.588T>A
NM_000238.3:c.365T>A , LRG_288t1:c.365T>A	NP_000229.1:p.Val122Asp
NM_172056.2:c.365T>A , LRG_288t2:c.365T>A	NP_742053.1:p.Val122Asp
XM_011516185.1:c.65T>A	XP_011514487.1:p.Val22Asp
XM_011516186.1:c.365T>A	XP_011514488.1:p.Val122Asp
XM_011516185.2:c.65T>A	XP_011514487.1:p.Val22Asp
XM_011516186.3:c.365T>A	XP_011514488.1:p.Val122Asp
XM_017012195.1:c.215T>A	XP_016867684.1:p.Val72Asp
XM_017012196.1:c.188T>A	XP_016867685.1:p.Val63Asp
NM_000238.4:c.365T>A MANE Select	NP_000229.1:p.Val122Asp