Canonical Allele Identifier: CA1303193818

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162380785A= , CM000664.2:g.162380785A=	GRCh38
NC_000002.11:g.163237295A= , CM000664.1:g.163237295A=	GRCh37
NC_000002.10:g.162945541A=	NCBI36
NG_041938.1:g.462963T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332142.10:c.2963-764T= MANE Select	ENSP00000331727.5:n.2963-764T=
ENST00000332142.9:c.2963-764T=	ENSP00000331727.5:n.2963-764T=
ENST00000618399.4:c.2663-764T=	ENSP00000482818.1:n.2663-764T=
NM_033272.3:c.2963-764T=	NP_150375.2:n.2963-764T=
XM_011512109.1:c.2987-764T=	XP_011510411.1:n.2987-764T=
XM_011512109.3:c.2987-764T=	XP_011510411.1:n.2987-764T=
XM_017005218.2:c.2978-764T=	XP_016860707.1:n.2978-764T=
XM_017005219.2:c.2954-764T=	XP_016860708.1:n.2954-764T=
XM_017005220.2:c.2942-764T=	XP_016860709.1:n.2942-764T=
NM_033272.4:c.2963-764T= MANE Select	NP_150375.2:n.2963-764T=