Canonical Allele Identifier: CA369852866

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644535C>G (hg19) ; chr7:g.150947447C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947447C>G , CM000669.2:g.150947447C>G	GRCh38
NC_000007.13:g.150644535C>G , CM000669.1:g.150644535C>G	GRCh37
NC_000007.12:g.150275468C>G	NCBI36
NG_008916.1:g.35480G>C , LRG_288:g.35480G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3866G>C
ENST00000262186.10:c.3033G>C MANE Select	ENSP00000262186.5:p.Glu1011Asp
ENST00000330883.9:c.2013G>C	ENSP00000328531.4:p.Glu671Asp
ENST00000262186.9:c.3033G>C	ENSP00000262186.5:p.Glu1011Asp
ENST00000330883.8:c.2013G>C	ENSP00000328531.4:p.Glu671Asp
NM_000238.3:c.3033G>C , LRG_288t1:c.3033G>C	NP_000229.1:p.Glu1011Asp
NM_172057.2:c.2013G>C , LRG_288t3:c.2013G>C	NP_742054.1:p.Glu671Asp
XM_011516185.1:c.2733G>C	XP_011514487.1:p.Glu911Asp
XM_011516186.1:c.*113G>C	XP_011514488.1:n.*113G>C
XM_011516185.2:c.2733G>C	XP_011514487.1:p.Glu911Asp
XM_011516186.3:c.*113G>C	XP_011514488.1:n.*113G>C
XM_017012195.1:c.2883G>C	XP_016867684.1:p.Glu961Asp
XM_017012196.1:c.2856G>C	XP_016867685.1:p.Glu952Asp
NM_000238.4:c.3033G>C MANE Select	NP_000229.1:p.Glu1011Asp
NM_172057.3:c.2013G>C	NP_742054.1:p.Glu671Asp