Canonical Allele Identifier: CA458644795

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644427G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947339G>C , CM000669.2:g.150947339G>C	GRCh38
NC_000007.13:g.150644427G>C , CM000669.1:g.150644427G>C	GRCh37
NC_000007.12:g.150275360G>C	NCBI36
NG_008916.1:g.35588C>G , LRG_288:g.35588C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3974C>G
ENST00000262186.10:c.3141C>G MANE Select	ENSP00000262186.5:p.Arg1047=
ENST00000330883.9:c.2121C>G	ENSP00000328531.4:p.Arg707=
ENST00000262186.9:c.3141C>G	ENSP00000262186.5:p.Arg1047=
ENST00000330883.8:c.2121C>G	ENSP00000328531.4:p.Arg707=
NM_000238.3:c.3141C>G , LRG_288t1:c.3141C>G	NP_000229.1:p.Arg1047=
NM_172057.2:c.2121C>G , LRG_288t3:c.2121C>G	NP_742054.1:p.Arg707=
XM_011516185.1:c.2841C>G	XP_011514487.1:p.Arg947=
XM_011516185.2:c.2841C>G	XP_011514487.1:p.Arg947=
XM_017012195.1:c.2991C>G	XP_016867684.1:p.Arg997=
XM_017012196.1:c.2964C>G	XP_016867685.1:p.Arg988=
NM_000238.4:c.3141C>G MANE Select	NP_000229.1:p.Arg1047=
NM_172057.3:c.2121C>G	NP_742054.1:p.Arg707=