Canonical Allele Identifier: CA349220872
Gene: KCNH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162435302G>A , CM000664.2:g.162435302G>A GRCh38
NC_000002.11:g.163291812G>A , CM000664.1:g.163291812G>A GRCh37
NC_000002.10:g.163000058G>A NCBI36
NG_041938.1:g.408446C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332142.10:c.1850C>T MANE Select ENSP00000331727.5:p.Ala617Val
ENST00000328032.8:c.1829C>T ENSP00000333781.4:p.Ala610Val
ENST00000332142.9:c.1850C>T ENSP00000331727.5:p.Ala617Val
ENST00000618399.4:c.1550C>T ENSP00000482818.1:p.Ala517Val
ENST00000621889.1:c.1523C>T ENSP00000483158.1:p.Ala508Val
NM_033272.3:c.1850C>T NP_150375.2:p.Ala617Val
NM_173162.2:c.1829C>T NP_775185.1:p.Ala610Val
XM_011512109.1:c.1874C>T XP_011510411.1:p.Ala625Val
XM_011512109.3:c.1874C>T XP_011510411.1:p.Ala625Val
XM_017005218.2:c.1874C>T XP_016860707.1:p.Ala625Val
XM_017005219.2:c.1850C>T XP_016860708.1:p.Ala617Val
XM_017005220.2:c.1829C>T XP_016860709.1:p.Ala610Val
XM_017005221.2:c.1874C>T XP_016860710.1:p.Ala625Val
NM_033272.4:c.1850C>T MANE Select NP_150375.2:p.Ala617Val
NM_173162.3:c.1829C>T NP_775185.1:p.Ala610Val