Canonical Allele Identifier: CA7727843
Community Standard Title: NM_198525.3(KIF7):c.3061C>T (p.Arg1021Cys)
Gene: KIF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89631545G>A , CM000677.2:g.89631545G>A GRCh38
NC_000015.9:g.90174776G>A , CM000677.1:g.90174776G>A GRCh37
NC_000015.8:g.87975780G>A NCBI36
NG_030338.1:g.28907C>T

Transcript Alleles

HGVS Amino-acid Change
NM_198525.3:c.3061C>T MANE Select NP_940927.2:p.Arg1021Cys
ENST00000394412.8:c.3061C>T MANE Select ENSP00000377934.3:p.Arg1021Cys
NM_198525.2:c.3061C>T NP_940927.2:p.Arg1021Cys
ENST00000394412.7:c.3061C>T ENSP00000377934.3:p.Arg1021Cys
ENST00000677187.1:n.735C>T
ENST00000696512.1:c.3184C>T ENSP00000512678.1:p.Arg1062Cys
XM_005254902.2:c.3061C>T XP_005254959.1:p.Arg1021Cys
XM_011521531.1:c.3184C>T XP_011519833.1:p.Arg1062Cys
XM_011521531.2:c.3184C>T XP_011519833.1:p.Arg1062Cys
XM_011521532.1:c.3181C>T XP_011519834.1:p.Arg1061Cys
XM_011521533.1:c.3181C>T XP_011519835.1:p.Arg1061Cys
XM_011521534.1:c.3184C>T XP_011519836.1:p.Arg1062Cys
XM_011521535.1:c.3184C>T XP_011519837.1:p.Arg1062Cys
XM_011521536.1:c.3184C>T XP_011519838.1:p.Arg1062Cys