Canonical Allele Identifier: CA1752461148

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974485C= , CM000669.2:g.150974485C=	GRCh38
NC_000007.13:g.150671573C= , CM000669.1:g.150671573C=	GRCh37
NC_000007.12:g.150302506C=	NCBI36
NG_008916.1:g.8442G= , LRG_288:g.8442G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.307+226G= MANE Select	ENSP00000262186.5:n.307+226G=
ENST00000262186.9:c.307+226G=	ENSP00000262186.5:n.307+226G=
ENST00000430723.4:c.130+226G=	ENSP00000387657.4:n.130+226G=
ENST00000532957.5:n.530+226G=
NM_000238.3:c.307+226G= , LRG_288t1:c.307+226G=	NP_000229.1:n.307+226G=
NM_172056.2:c.307+226G= , LRG_288t2:c.307+226G=	NP_742053.1:n.307+226G=
XM_011516186.1:c.307+226G=	XP_011514488.1:n.307+226G=
XM_011516185.2:c.-109G=	XP_011514487.1:n.-109G=
XM_011516186.3:c.307+226G=	XP_011514488.1:n.307+226G=
XM_017012196.1:c.130+226G=	XP_016867685.1:n.130+226G=
NM_000238.4:c.307+226G= MANE Select	NP_000229.1:n.307+226G=