Canonical Allele Identifier: CA349220794
Gene: KCNH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162435269A>G , CM000664.2:g.162435269A>G GRCh38
NC_000002.11:g.163291779A>G , CM000664.1:g.163291779A>G GRCh37
NC_000002.10:g.163000025A>G NCBI36
NG_041938.1:g.408479T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332142.10:c.1883T>C MANE Select ENSP00000331727.5:p.Val628Ala
ENST00000328032.8:c.1862T>C ENSP00000333781.4:p.Val621Ala
ENST00000332142.9:c.1883T>C ENSP00000331727.5:p.Val628Ala
ENST00000618399.4:c.1583T>C ENSP00000482818.1:p.Val528Ala
ENST00000621889.1:c.1556T>C ENSP00000483158.1:p.Val519Ala
NM_033272.3:c.1883T>C NP_150375.2:p.Val628Ala
NM_173162.2:c.1862T>C NP_775185.1:p.Val621Ala
XM_011512109.1:c.1907T>C XP_011510411.1:p.Val636Ala
XM_011512109.3:c.1907T>C XP_011510411.1:p.Val636Ala
XM_017005218.2:c.1907T>C XP_016860707.1:p.Val636Ala
XM_017005219.2:c.1883T>C XP_016860708.1:p.Val628Ala
XM_017005220.2:c.1862T>C XP_016860709.1:p.Val621Ala
XM_017005221.2:c.1907T>C XP_016860710.1:p.Val636Ala
NM_033272.4:c.1883T>C MANE Select NP_150375.2:p.Val628Ala
NM_173162.3:c.1862T>C NP_775185.1:p.Val621Ala