Canonical Allele Identifier: CA1752446550

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977916T= , CM000669.2:g.150977916T=	GRCh38
NC_000007.13:g.150675004T= , CM000669.1:g.150675004T=	GRCh37
NC_000007.12:g.150305937T=	NCBI36
NG_008916.1:g.5011A= , LRG_288:g.5011A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.-3A= MANE Select	ENSP00000262186.5:n.-3A=
ENST00000262186.9:c.-3A=	ENSP00000262186.5:n.-3A=
ENST00000430723.4:c.-180A=	ENSP00000387657.4:n.-180A=
ENST00000532957.5:n.221A=
NM_000238.3:c.-3A= , LRG_288t1:c.-3A=	NP_000229.1:n.-3A=
NM_172056.2:c.-3A= , LRG_288t2:c.-3A=	NP_742053.1:n.-3A=
XM_011516186.1:c.-3A=	XP_011514488.1:n.-3A=
XM_011516186.3:c.-3A=	XP_011514488.1:n.-3A=
NM_000238.4:c.-3A= MANE Select	NP_000229.1:n.-3A=