Canonical Allele Identifier: CA458645195

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646091A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949003A>C , CM000669.2:g.150949003A>C	GRCh38
NC_000007.13:g.150646091A>C , CM000669.1:g.150646091A>C	GRCh37
NC_000007.12:g.150277024A>C	NCBI36
NG_008916.1:g.33924T>G , LRG_288:g.33924T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3278T>G
ENST00000262186.10:c.2445T>G MANE Select	ENSP00000262186.5:p.Pro815=
ENST00000330883.9:c.1425T>G	ENSP00000328531.4:p.Pro475=
ENST00000262186.9:c.2445T>G	ENSP00000262186.5:p.Pro815=
ENST00000330883.8:c.1425T>G	ENSP00000328531.4:p.Pro475=
NM_000238.3:c.2445T>G , LRG_288t1:c.2445T>G	NP_000229.1:p.Pro815=
NM_172057.2:c.1425T>G , LRG_288t3:c.1425T>G	NP_742054.1:p.Pro475=
XM_011516185.1:c.2145T>G	XP_011514487.1:p.Pro715=
XM_011516186.1:c.2445T>G	XP_011514488.1:p.Pro815=
XM_011516185.2:c.2145T>G	XP_011514487.1:p.Pro715=
XM_011516186.3:c.2445T>G	XP_011514488.1:p.Pro815=
XM_017012195.1:c.2295T>G	XP_016867684.1:p.Pro765=
XM_017012196.1:c.2268T>G	XP_016867685.1:p.Pro756=
NM_000238.4:c.2445T>G MANE Select	NP_000229.1:p.Pro815=
NM_172057.3:c.1425T>G	NP_742054.1:p.Pro475=