Canonical Allele Identifier: CA369861851

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654558T>A (hg19) ; chr7:g.150957470T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957470T>A , CM000669.2:g.150957470T>A	GRCh38
NC_000007.13:g.150654558T>A , CM000669.1:g.150654558T>A	GRCh37
NC_000007.12:g.150285491T>A	NCBI36
NG_008916.1:g.25457A>T , LRG_288:g.25457A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1782A>T
ENST00000262186.10:c.949A>T MANE Select	ENSP00000262186.5:p.Asn317Tyr
ENST00000262186.9:c.949A>T	ENSP00000262186.5:p.Asn317Tyr
ENST00000430723.4:c.601A>T	ENSP00000387657.4:p.Asn201Tyr
ENST00000532957.5:n.1172A>T
NM_000238.3:c.949A>T , LRG_288t1:c.949A>T	NP_000229.1:p.Asn317Tyr
NM_172056.2:c.949A>T , LRG_288t2:c.949A>T	NP_742053.1:p.Asn317Tyr
XM_011516185.1:c.649A>T	XP_011514487.1:p.Asn217Tyr
XM_011516186.1:c.949A>T	XP_011514488.1:p.Asn317Tyr
XM_011516185.2:c.649A>T	XP_011514487.1:p.Asn217Tyr
XM_011516186.3:c.949A>T	XP_011514488.1:p.Asn317Tyr
XM_017012195.1:c.799A>T	XP_016867684.1:p.Asn267Tyr
XM_017012196.1:c.772A>T	XP_016867685.1:p.Asn258Tyr
NM_000238.4:c.949A>T MANE Select	NP_000229.1:p.Asn317Tyr