Canonical Allele Identifier: CA2685605081

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150950481-T-TCCACCATCCCACACTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950481_150950482insCCACCATCCCACACTCC , CM000669.2:g.150950481_150950482insCCACCATCCCACACTCC	GRCh38
NC_000007.13:g.150647569_150647570insCCACCATCCCACACTCC , CM000669.1:g.150647569_150647570insCCACCATCCCACACTCC	GRCh37
NC_000007.12:g.150278502_150278503insCCACCATCCCACACTCC	NCBI36
NG_008916.1:g.32445_32446insGGAGTGTGGGATGGTGG , LRG_288:g.32445_32446insGGAGTGTGGGATGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1444-62_1444-61insGGAGTGTGGGATGGTGG
ENST00000684241.1:n.2979-62_2979-61insGGAGTGTGGGATGGTGG
ENST00000262186.10:c.2146-62_2146-61insGGAGTGTGGGATGGTGG MANE Select	ENSP00000262186.5:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
ENST00000330883.9:c.1126-62_1126-61insGGAGTGTGGGATGGTGG	ENSP00000328531.4:n.1126-62_1126-61insGGAGTGTGGGATGGTGG
ENST00000262186.9:c.2146-62_2146-61insGGAGTGTGGGATGGTGG	ENSP00000262186.5:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
ENST00000330883.8:c.1126-62_1126-61insGGAGTGTGGGATGGTGG	ENSP00000328531.4:n.1126-62_1126-61insGGAGTGTGGGATGGTGG
ENST00000430723.4:c.1798-62_1798-61insGGAGTGTGGGATGGTGG	ENSP00000387657.4:n.1798-62_1798-61insGGAGTGTGGGATGGTGG
ENST00000461280.1:n.1433-62_1433-61insGGAGTGTGGGATGGTGG
ENST00000473610.5:n.1778-62_1778-61insGGAGTGTGGGATGGTGG
ENST00000532957.5:n.2369-62_2369-61insGGAGTGTGGGATGGTGG
NM_000238.3:c.2146-62_2146-61insGGAGTGTGGGATGGTGG , LRG_288t1:c.2146-62_2146-61insGGAGTGTGGGATGGTGG	NP_000229.1:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
NM_001204798.1:c.1126-62_1126-61insGGAGTGTGGGATGGTGG	NP_001191727.1:n.1126-62_1126-61insGGAGTGTGGGATGGTGG
NM_172056.2:c.2146-62_2146-61insGGAGTGTGGGATGGTGG , LRG_288t2:c.2146-62_2146-61insGGAGTGTGGGATGGTGG	NP_742053.1:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
NM_172057.2:c.1126-62_1126-61insGGAGTGTGGGATGGTGG , LRG_288t3:c.1126-62_1126-61insGGAGTGTGGGATGGTGG	NP_742054.1:n.1126-62_1126-61insGGAGTGTGGGATGGTGG
XM_011516185.1:c.1846-62_1846-61insGGAGTGTGGGATGGTGG	XP_011514487.1:n.1846-62_1846-61insGGAGTGTGGGATGGTGG
XM_011516186.1:c.2146-62_2146-61insGGAGTGTGGGATGGTGG	XP_011514488.1:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
XM_011516185.2:c.1846-62_1846-61insGGAGTGTGGGATGGTGG	XP_011514487.1:n.1846-62_1846-61insGGAGTGTGGGATGGTGG
XM_011516186.3:c.2146-62_2146-61insGGAGTGTGGGATGGTGG	XP_011514488.1:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
XM_017012195.1:c.1996-62_1996-61insGGAGTGTGGGATGGTGG	XP_016867684.1:n.1996-62_1996-61insGGAGTGTGGGATGGTGG
XM_017012196.1:c.1969-62_1969-61insGGAGTGTGGGATGGTGG	XP_016867685.1:n.1969-62_1969-61insGGAGTGTGGGATGGTGG
NM_000238.4:c.2146-62_2146-61insGGAGTGTGGGATGGTGG MANE Select	NP_000229.1:n.2146-62_2146-61insGGAGTGTGGGATGGTGG
NM_001204798.2:c.1126-62_1126-61insGGAGTGTGGGATGGTGG	NP_001191727.1:n.1126-62_1126-61insGGAGTGTGGGATGGTGG
NM_172057.3:c.1126-62_1126-61insGGAGTGTGGGATGGTGG	NP_742054.1:n.1126-62_1126-61insGGAGTGTGGGATGGTGG