Canonical Allele Identifier: CA369861684

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654509A>C (hg19) ; chr7:g.150957421A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957421A>C , CM000669.2:g.150957421A>C	GRCh38
NC_000007.13:g.150654509A>C , CM000669.1:g.150654509A>C	GRCh37
NC_000007.12:g.150285442A>C	NCBI36
NG_008916.1:g.25506T>G , LRG_288:g.25506T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1831T>G
ENST00000262186.10:c.998T>G MANE Select	ENSP00000262186.5:p.Ile333Ser
ENST00000262186.9:c.998T>G	ENSP00000262186.5:p.Ile333Ser
ENST00000430723.4:c.650T>G	ENSP00000387657.4:p.Ile217Ser
ENST00000532957.5:n.1221T>G
NM_000238.3:c.998T>G , LRG_288t1:c.998T>G	NP_000229.1:p.Ile333Ser
NM_172056.2:c.998T>G , LRG_288t2:c.998T>G	NP_742053.1:p.Ile333Ser
XM_011516185.1:c.698T>G	XP_011514487.1:p.Ile233Ser
XM_011516186.1:c.998T>G	XP_011514488.1:p.Ile333Ser
XM_011516185.2:c.698T>G	XP_011514487.1:p.Ile233Ser
XM_011516186.3:c.998T>G	XP_011514488.1:p.Ile333Ser
XM_017012195.1:c.848T>G	XP_016867684.1:p.Ile283Ser
XM_017012196.1:c.821T>G	XP_016867685.1:p.Ile274Ser
NM_000238.4:c.998T>G MANE Select	NP_000229.1:p.Ile333Ser