Canonical Allele Identifier: CA1303221322

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162435403G= , CM000664.2:g.162435403G=	GRCh38
NC_000002.11:g.163291913G= , CM000664.1:g.163291913G=	GRCh37
NC_000002.10:g.163000159G=	NCBI36
NG_041938.1:g.408345C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.1749C= MANE Select	ENSP00000331727.5:p.Asp583=
ENST00000328032.8:c.1728C=	ENSP00000333781.4:p.Asp576=
ENST00000332142.9:c.1749C=	ENSP00000331727.5:p.Asp583=
ENST00000618399.4:c.1449C=	ENSP00000482818.1:p.Asp483=
ENST00000621889.1:c.1422C=	ENSP00000483158.1:p.Asp474=
NM_033272.3:c.1749C=	NP_150375.2:p.Asp583=
NM_173162.2:c.1728C=	NP_775185.1:p.Asp576=
XM_011512109.1:c.1773C=	XP_011510411.1:p.Asp591=
XM_011512109.3:c.1773C=	XP_011510411.1:p.Asp591=
XM_017005218.2:c.1773C=	XP_016860707.1:p.Asp591=
XM_017005219.2:c.1749C=	XP_016860708.1:p.Asp583=
XM_017005220.2:c.1728C=	XP_016860709.1:p.Asp576=
XM_017005221.2:c.1773C=	XP_016860710.1:p.Asp591=
NM_033272.4:c.1749C= MANE Select	NP_150375.2:p.Asp583=
NM_173162.3:c.1728C=	NP_775185.1:p.Asp576=