Canonical Allele Identifier: CA7727951
Gene: KIF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89632939G>T , CM000677.2:g.89632939G>T GRCh38
NC_000015.9:g.90176170G>T , CM000677.1:g.90176170G>T GRCh37
NC_000015.8:g.87977174G>T NCBI36
NG_030338.1:g.27513C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696512.1:c.2899C>A ENSP00000512678.1:p.Arg967=
ENST00000394412.8:c.2776C>A MANE Select ENSP00000377934.3:p.Arg926=
ENST00000677187.1:n.450C>A
ENST00000394412.7:c.2776C>A ENSP00000377934.3:p.Arg926=
NM_198525.2:c.2776C>A NP_940927.2:p.Arg926=
XM_005254902.2:c.2776C>A XP_005254959.1:p.Arg926=
XM_011521531.1:c.2899C>A XP_011519833.1:p.Arg967=
XM_011521532.1:c.2896C>A XP_011519834.1:p.Arg966=
XM_011521533.1:c.2896C>A XP_011519835.1:p.Arg966=
XM_011521534.1:c.2899C>A XP_011519836.1:p.Arg967=
XM_011521535.1:c.2899C>A XP_011519837.1:p.Arg967=
XM_011521536.1:c.2899C>A XP_011519838.1:p.Arg967=
XM_011521531.2:c.2899C>A XP_011519833.1:p.Arg967=
NM_198525.3:c.2776C>A MANE Select NP_940927.2:p.Arg926=