Canonical Allele Identifier: CA1752446476

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977885G= , CM000669.2:g.150977885G=	GRCh38
NC_000007.13:g.150674973G= , CM000669.1:g.150674973G=	GRCh37
NC_000007.12:g.150305906G=	NCBI36
NG_008916.1:g.5042C= , LRG_288:g.5042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.29C= MANE Select	ENSP00000262186.5:p.Pro10=
ENST00000262186.9:c.29C=	ENSP00000262186.5:p.Pro10=
ENST00000430723.4:c.-149C=	ENSP00000387657.4:n.-149C=
ENST00000532957.5:n.252C=
NM_000238.3:c.29C= , LRG_288t1:c.29C=	NP_000229.1:p.Pro10=
NM_172056.2:c.29C= , LRG_288t2:c.29C=	NP_742053.1:p.Pro10=
XM_011516186.1:c.29C=	XP_011514488.1:p.Pro10=
XM_011516186.3:c.29C=	XP_011514488.1:p.Pro10=
NM_000238.4:c.29C= MANE Select	NP_000229.1:p.Pro10=