Canonical Allele Identifier: CA2141919947

Gene: KCNH5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.62855629A= , CM000676.2:g.62855629A=	GRCh38
NC_000014.8:g.63322347A= , CM000676.1:g.63322347A=	GRCh37
NC_000014.7:g.62392100A=	NCBI36
NG_034062.1:g.194610T=

Transcript Alleles

HGVS	Amino-acid Change
NM_139318.5:c.1370-5777T= MANE Select	NP_647479.2:n.1370-5777T=
ENST00000322893.12:c.1370-5777T= MANE Select	ENSP00000321427.7:n.1370-5777T=
NM_139318.4:c.1370-5777T=	NP_647479.2:n.1370-5777T=
NM_172375.2:c.1370-5777T=	NP_758963.1:n.1370-5777T=
NM_172375.3:c.1370-5777T=	NP_758963.1:n.1370-5777T=
ENST00000322893.11:c.1370-5777T=	ENSP00000321427.7:n.1370-5777T=
ENST00000394968.2:c.1196-5777T=	ENSP00000378419.1:n.1196-5777T=
ENST00000420622.6:c.1370-5777T=	ENSP00000395439.2:n.1370-5777T=
XM_011536658.1:c.1370-5777T=	XP_011534960.1:n.1370-5777T=