Canonical Allele Identifier: CA349223674

Gene: KCNH7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162836569C>T , CM000664.2:g.162836569C>T	GRCh38
NC_000002.11:g.163693079C>T , CM000664.1:g.163693079C>T	GRCh37
NC_000002.10:g.163401325C>T	NCBI36
NG_041938.1:g.7179G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332142.10:c.275G>A MANE Select	ENSP00000331727.5:p.Arg92Lys
ENST00000328032.8:c.275G>A	ENSP00000333781.4:p.Arg92Lys
ENST00000332142.9:c.275G>A	ENSP00000331727.5:p.Arg92Lys
NM_033272.3:c.275G>A	NP_150375.2:p.Arg92Lys
NM_173162.2:c.275G>A	NP_775185.1:p.Arg92Lys
XM_011512109.1:c.275G>A	XP_011510411.1:p.Arg92Lys
XM_011512109.3:c.275G>A	XP_011510411.1:p.Arg92Lys
XM_017005218.2:c.275G>A	XP_016860707.1:p.Arg92Lys
XM_017005219.2:c.275G>A	XP_016860708.1:p.Arg92Lys
XM_017005220.2:c.275G>A	XP_016860709.1:p.Arg92Lys
XM_017005221.2:c.275G>A	XP_016860710.1:p.Arg92Lys
NM_033272.4:c.275G>A MANE Select	NP_150375.2:p.Arg92Lys
NM_173162.3:c.275G>A	NP_775185.1:p.Arg92Lys