Canonical Allele Identifier: CA369852697

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644483T>A (hg19) ; chr7:g.150947395T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947395T>A , CM000669.2:g.150947395T>A	GRCh38
NC_000007.13:g.150644483T>A , CM000669.1:g.150644483T>A	GRCh37
NC_000007.12:g.150275416T>A	NCBI36
NG_008916.1:g.35532A>T , LRG_288:g.35532A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3918A>T
ENST00000262186.10:c.3085A>T MANE Select	ENSP00000262186.5:p.Ser1029Cys
ENST00000330883.9:c.2065A>T	ENSP00000328531.4:p.Ser689Cys
ENST00000262186.9:c.3085A>T	ENSP00000262186.5:p.Ser1029Cys
ENST00000330883.8:c.2065A>T	ENSP00000328531.4:p.Ser689Cys
NM_000238.3:c.3085A>T , LRG_288t1:c.3085A>T	NP_000229.1:p.Ser1029Cys
NM_172057.2:c.2065A>T , LRG_288t3:c.2065A>T	NP_742054.1:p.Ser689Cys
XM_011516185.1:c.2785A>T	XP_011514487.1:p.Ser929Cys
XM_011516185.2:c.2785A>T	XP_011514487.1:p.Ser929Cys
XM_017012195.1:c.2935A>T	XP_016867684.1:p.Ser979Cys
XM_017012196.1:c.2908A>T	XP_016867685.1:p.Ser970Cys
NM_000238.4:c.3085A>T MANE Select	NP_000229.1:p.Ser1029Cys
NM_172057.3:c.2065A>T	NP_742054.1:p.Ser689Cys