Canonical Allele Identifier: CA369861789

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654542G>T (hg19) ; chr7:g.150957454G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957454G>T , CM000669.2:g.150957454G>T	GRCh38
NC_000007.13:g.150654542G>T , CM000669.1:g.150654542G>T	GRCh37
NC_000007.12:g.150285475G>T	NCBI36
NG_008916.1:g.25473C>A , LRG_288:g.25473C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1798C>A
ENST00000262186.10:c.965C>A MANE Select	ENSP00000262186.5:p.Ser322Tyr
ENST00000262186.9:c.965C>A	ENSP00000262186.5:p.Ser322Tyr
ENST00000430723.4:c.617C>A	ENSP00000387657.4:p.Ser206Tyr
ENST00000532957.5:n.1188C>A
NM_000238.3:c.965C>A , LRG_288t1:c.965C>A	NP_000229.1:p.Ser322Tyr
NM_172056.2:c.965C>A , LRG_288t2:c.965C>A	NP_742053.1:p.Ser322Tyr
XM_011516185.1:c.665C>A	XP_011514487.1:p.Ser222Tyr
XM_011516186.1:c.965C>A	XP_011514488.1:p.Ser322Tyr
XM_011516185.2:c.665C>A	XP_011514487.1:p.Ser222Tyr
XM_011516186.3:c.965C>A	XP_011514488.1:p.Ser322Tyr
XM_017012195.1:c.815C>A	XP_016867684.1:p.Ser272Tyr
XM_017012196.1:c.788C>A	XP_016867685.1:p.Ser263Tyr
NM_000238.4:c.965C>A MANE Select	NP_000229.1:p.Ser322Tyr