Canonical Allele Identifier: CA369854668

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645944A>C (hg19) ; chr7:g.150948856A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948856A>C , CM000669.2:g.150948856A>C	GRCh38
NC_000007.13:g.150645944A>C , CM000669.1:g.150645944A>C	GRCh37
NC_000007.12:g.150276877A>C	NCBI36
NG_008916.1:g.34071T>G , LRG_288:g.34071T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3425T>G
ENST00000262186.10:c.2592T>G MANE Select	ENSP00000262186.5:p.Asp864Glu
ENST00000330883.9:c.1572T>G	ENSP00000328531.4:p.Asp524Glu
ENST00000262186.9:c.2592T>G	ENSP00000262186.5:p.Asp864Glu
ENST00000330883.8:c.1572T>G	ENSP00000328531.4:p.Asp524Glu
NM_000238.3:c.2592T>G , LRG_288t1:c.2592T>G	NP_000229.1:p.Asp864Glu
NM_172057.2:c.1572T>G , LRG_288t3:c.1572T>G	NP_742054.1:p.Asp524Glu
XM_011516185.1:c.2292T>G	XP_011514487.1:p.Asp764Glu
XM_011516186.1:c.2592T>G	XP_011514488.1:p.Asp864Glu
XM_011516185.2:c.2292T>G	XP_011514487.1:p.Asp764Glu
XM_011516186.3:c.2592T>G	XP_011514488.1:p.Asp864Glu
XM_017012195.1:c.2442T>G	XP_016867684.1:p.Asp814Glu
XM_017012196.1:c.2415T>G	XP_016867685.1:p.Asp805Glu
NM_000238.4:c.2592T>G MANE Select	NP_000229.1:p.Asp864Glu
NM_172057.3:c.1572T>G	NP_742054.1:p.Asp524Glu