Canonical Allele Identifier: CA369855017

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646029T>A (hg19) ; chr7:g.150948941T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948941T>A , CM000669.2:g.150948941T>A	GRCh38
NC_000007.13:g.150646029T>A , CM000669.1:g.150646029T>A	GRCh37
NC_000007.12:g.150276962T>A	NCBI36
NG_008916.1:g.33986A>T , LRG_288:g.33986A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3340A>T
ENST00000262186.10:c.2507A>T MANE Select	ENSP00000262186.5:p.Asp836Val
ENST00000330883.9:c.1487A>T	ENSP00000328531.4:p.Asp496Val
ENST00000262186.9:c.2507A>T	ENSP00000262186.5:p.Asp836Val
ENST00000330883.8:c.1487A>T	ENSP00000328531.4:p.Asp496Val
NM_000238.3:c.2507A>T , LRG_288t1:c.2507A>T	NP_000229.1:p.Asp836Val
NM_172057.2:c.1487A>T , LRG_288t3:c.1487A>T	NP_742054.1:p.Asp496Val
XM_011516185.1:c.2207A>T	XP_011514487.1:p.Asp736Val
XM_011516186.1:c.2507A>T	XP_011514488.1:p.Asp836Val
XM_011516185.2:c.2207A>T	XP_011514487.1:p.Asp736Val
XM_011516186.3:c.2507A>T	XP_011514488.1:p.Asp836Val
XM_017012195.1:c.2357A>T	XP_016867684.1:p.Asp786Val
XM_017012196.1:c.2330A>T	XP_016867685.1:p.Asp777Val
NM_000238.4:c.2507A>T MANE Select	NP_000229.1:p.Asp836Val
NM_172057.3:c.1487A>T	NP_742054.1:p.Asp496Val