Canonical Allele Identifier: CA369865791

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150671952A>T (hg19) ; chr7:g.150974864A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974864A>T , CM000669.2:g.150974864A>T	GRCh38
NC_000007.13:g.150671952A>T , CM000669.1:g.150671952A>T	GRCh37
NC_000007.12:g.150302885A>T	NCBI36
NG_008916.1:g.8063T>A , LRG_288:g.8063T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.154T>A MANE Select	ENSP00000262186.5:p.Cys52Ser
ENST00000262186.9:c.154T>A	ENSP00000262186.5:p.Cys52Ser
ENST00000430723.4:c.-24T>A	ENSP00000387657.4:n.-24T>A
ENST00000532957.5:n.377T>A
NM_000238.3:c.154T>A , LRG_288t1:c.154T>A	NP_000229.1:p.Cys52Ser
NM_172056.2:c.154T>A , LRG_288t2:c.154T>A	NP_742053.1:p.Cys52Ser
XM_011516186.1:c.154T>A	XP_011514488.1:p.Cys52Ser
XM_011516186.3:c.154T>A	XP_011514488.1:p.Cys52Ser
XM_017012196.1:c.-24T>A	XP_016867685.1:n.-24T>A
NM_000238.4:c.154T>A MANE Select	NP_000229.1:p.Cys52Ser