Canonical Allele Identifier: CA369852508

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947338-G-C
• MyVariant Identifiers: chr7:g.150644426G>C (hg19) ; chr7:g.150947338G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947338G>C , CM000669.2:g.150947338G>C	GRCh38
NC_000007.13:g.150644426G>C , CM000669.1:g.150644426G>C	GRCh37
NC_000007.12:g.150275359G>C	NCBI36
NG_008916.1:g.35589C>G , LRG_288:g.35589C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3975C>G
ENST00000262186.10:c.3142C>G MANE Select	ENSP00000262186.5:p.Gln1048Glu
ENST00000330883.9:c.2122C>G	ENSP00000328531.4:p.Gln708Glu
ENST00000262186.9:c.3142C>G	ENSP00000262186.5:p.Gln1048Glu
ENST00000330883.8:c.2122C>G	ENSP00000328531.4:p.Gln708Glu
NM_000238.3:c.3142C>G , LRG_288t1:c.3142C>G	NP_000229.1:p.Gln1048Glu
NM_172057.2:c.2122C>G , LRG_288t3:c.2122C>G	NP_742054.1:p.Gln708Glu
XM_011516185.1:c.2842C>G	XP_011514487.1:p.Gln948Glu
XM_011516185.2:c.2842C>G	XP_011514487.1:p.Gln948Glu
XM_017012195.1:c.2992C>G	XP_016867684.1:p.Gln998Glu
XM_017012196.1:c.2965C>G	XP_016867685.1:p.Gln989Glu
NM_000238.4:c.3142C>G MANE Select	NP_000229.1:p.Gln1048Glu
NM_172057.3:c.2122C>G	NP_742054.1:p.Gln708Glu