Canonical Allele Identifier: CA1752420205

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959772A= , CM000669.2:g.150959772A=	GRCh38
NC_000007.13:g.150656860A= , CM000669.1:g.150656860A=	GRCh37
NC_000007.12:g.150287793A=	NCBI36
NG_008916.1:g.23155T= , LRG_288:g.23155T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1105T=
ENST00000262186.10:c.308-36T= MANE Select	ENSP00000262186.5:n.308-36T=
ENST00000262186.9:c.308-36T=	ENSP00000262186.5:n.308-36T=
ENST00000430723.4:c.131-36T=	ENSP00000387657.4:n.131-36T=
ENST00000532957.5:n.531-36T=
NM_000238.3:c.308-36T= , LRG_288t1:c.308-36T=	NP_000229.1:n.308-36T=
NM_172056.2:c.308-36T= , LRG_288t2:c.308-36T=	NP_742053.1:n.308-36T=
XM_011516185.1:c.8-36T=	XP_011514487.1:n.8-36T=
XM_011516186.1:c.308-36T=	XP_011514488.1:n.308-36T=
XM_011516185.2:c.8-36T=	XP_011514487.1:n.8-36T=
XM_011516186.3:c.308-36T=	XP_011514488.1:n.308-36T=
XM_017012195.1:c.158-36T=	XP_016867684.1:n.158-36T=
XM_017012196.1:c.131-36T=	XP_016867685.1:n.131-36T=
NM_000238.4:c.308-36T= MANE Select	NP_000229.1:n.308-36T=