Canonical Allele Identifier: CA1303221319

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162435385A= , CM000664.2:g.162435385A=	GRCh38
NC_000002.11:g.163291895A= , CM000664.1:g.163291895A=	GRCh37
NC_000002.10:g.163000141A=	NCBI36
NG_041938.1:g.408363T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.1767T= MANE Select	ENSP00000331727.5:p.Asp589=
ENST00000328032.8:c.1746T=	ENSP00000333781.4:p.Asp582=
ENST00000332142.9:c.1767T=	ENSP00000331727.5:p.Asp589=
ENST00000618399.4:c.1467T=	ENSP00000482818.1:p.Asp489=
ENST00000621889.1:c.1440T=	ENSP00000483158.1:p.Asp480=
NM_033272.3:c.1767T=	NP_150375.2:p.Asp589=
NM_173162.2:c.1746T=	NP_775185.1:p.Asp582=
XM_011512109.1:c.1791T=	XP_011510411.1:p.Asp597=
XM_011512109.3:c.1791T=	XP_011510411.1:p.Asp597=
XM_017005218.2:c.1791T=	XP_016860707.1:p.Asp597=
XM_017005219.2:c.1767T=	XP_016860708.1:p.Asp589=
XM_017005220.2:c.1746T=	XP_016860709.1:p.Asp582=
XM_017005221.2:c.1791T=	XP_016860710.1:p.Asp597=
NM_033272.4:c.1767T= MANE Select	NP_150375.2:p.Asp589=
NM_173162.3:c.1746T=	NP_775185.1:p.Asp582=