Canonical Allele Identifier: CA1752445393

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977349C= , CM000669.2:g.150977349C=	GRCh38
NC_000007.13:g.150674437C= , CM000669.1:g.150674437C=	GRCh37
NC_000007.12:g.150305370C=	NCBI36
NG_008916.1:g.5578G= , LRG_288:g.5578G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.76+489G= MANE Select	ENSP00000262186.5:n.76+489G=
ENST00000262186.9:c.76+489G=	ENSP00000262186.5:n.76+489G=
ENST00000430723.4:c.-102+489G=	ENSP00000387657.4:n.-102+489G=
ENST00000532957.5:n.299+489G=
NM_000238.3:c.76+489G= , LRG_288t1:c.76+489G=	NP_000229.1:n.76+489G=
NM_172056.2:c.76+489G= , LRG_288t2:c.76+489G=	NP_742053.1:n.76+489G=
XM_011516186.1:c.76+489G=	XP_011514488.1:n.76+489G=
XM_011516186.3:c.76+489G=	XP_011514488.1:n.76+489G=
NM_000238.4:c.76+489G= MANE Select	NP_000229.1:n.76+489G=