Canonical Allele Identifier: CA458646814

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655520C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958432C>G , CM000669.2:g.150958432C>G	GRCh38
NC_000007.13:g.150655520C>G , CM000669.1:g.150655520C>G	GRCh37
NC_000007.12:g.150286453C>G	NCBI36
NG_008916.1:g.24495G>C , LRG_288:g.24495G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1376G>C
ENST00000262186.10:c.543G>C MANE Select	ENSP00000262186.5:p.Arg181=
ENST00000262186.9:c.543G>C	ENSP00000262186.5:p.Arg181=
ENST00000430723.4:c.235-40G>C	ENSP00000387657.4:n.235-40G>C
ENST00000532957.5:n.766G>C
NM_000238.3:c.543G>C , LRG_288t1:c.543G>C	NP_000229.1:p.Arg181=
NM_172056.2:c.543G>C , LRG_288t2:c.543G>C	NP_742053.1:p.Arg181=
XM_011516185.1:c.243G>C	XP_011514487.1:p.Arg81=
XM_011516186.1:c.543G>C	XP_011514488.1:p.Arg181=
XM_011516185.2:c.243G>C	XP_011514487.1:p.Arg81=
XM_011516186.3:c.543G>C	XP_011514488.1:p.Arg181=
XM_017012195.1:c.393G>C	XP_016867684.1:p.Arg131=
XM_017012196.1:c.366G>C	XP_016867685.1:p.Arg122=
NM_000238.4:c.543G>C MANE Select	NP_000229.1:p.Arg181=