Canonical Allele Identifier: CA458645927

Gene: KCNH2

Linked Data

• COSMIC: COSM6012992 ; COSM6012993
• MyVariant Identifiers: chr7:g.150654397G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957309G>C , CM000669.2:g.150957309G>C	GRCh38
NC_000007.13:g.150654397G>C , CM000669.1:g.150654397G>C	GRCh37
NC_000007.12:g.150285330G>C	NCBI36
NG_008916.1:g.25618C>G , LRG_288:g.25618C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1943C>G
ENST00000262186.10:c.1110C>G MANE Select	ENSP00000262186.5:p.Val370=
ENST00000262186.9:c.1110C>G	ENSP00000262186.5:p.Val370=
ENST00000430723.4:c.762C>G	ENSP00000387657.4:p.Val254=
ENST00000532957.5:n.1333C>G
NM_000238.3:c.1110C>G , LRG_288t1:c.1110C>G	NP_000229.1:p.Val370=
NM_172056.2:c.1110C>G , LRG_288t2:c.1110C>G	NP_742053.1:p.Val370=
XM_011516185.1:c.810C>G	XP_011514487.1:p.Val270=
XM_011516186.1:c.1110C>G	XP_011514488.1:p.Val370=
XM_011516185.2:c.810C>G	XP_011514487.1:p.Val270=
XM_011516186.3:c.1110C>G	XP_011514488.1:p.Val370=
XM_017012195.1:c.960C>G	XP_016867684.1:p.Val320=
XM_017012196.1:c.933C>G	XP_016867685.1:p.Val311=
NM_000238.4:c.1110C>G MANE Select	NP_000229.1:p.Val370=