Canonical Allele Identifier: CA1752419946

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959635T= , CM000669.2:g.150959635T=	GRCh38
NC_000007.13:g.150656723T= , CM000669.1:g.150656723T=	GRCh37
NC_000007.12:g.150287656T=	NCBI36
NG_008916.1:g.23292A= , LRG_288:g.23292A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1242A=
ENST00000262186.10:c.409A= MANE Select	ENSP00000262186.5:p.Met137=
ENST00000262186.9:c.409A=	ENSP00000262186.5:p.Met137=
ENST00000430723.4:c.232A=	ENSP00000387657.4:p.Met78=
ENST00000532957.5:n.632A=
NM_000238.3:c.409A= , LRG_288t1:c.409A=	NP_000229.1:p.Met137=
NM_172056.2:c.409A= , LRG_288t2:c.409A=	NP_742053.1:p.Met137=
XM_011516185.1:c.109A=	XP_011514487.1:p.Met37=
XM_011516186.1:c.409A=	XP_011514488.1:p.Met137=
XM_011516185.2:c.109A=	XP_011514487.1:p.Met37=
XM_011516186.3:c.409A=	XP_011514488.1:p.Met137=
XM_017012195.1:c.259A=	XP_016867684.1:p.Met87=
XM_017012196.1:c.232A=	XP_016867685.1:p.Met78=
NM_000238.4:c.409A= MANE Select	NP_000229.1:p.Met137=