Canonical Allele Identifier: CA2731483685
Gene: KIF7 HGNC NCBI

Linked Data

dbSNP Id: rs2141998190

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89631621_89631641dup , CM000677.2:g.89631621_89631641dup GRCh38
NC_000015.9:g.90174852_90174872dup , CM000677.1:g.90174852_90174872dup GRCh37
NC_000015.8:g.87975856_87975876dup NCBI36
NG_030338.1:g.28815_28835dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696512.1:c.3092_3112dup ENSP00000512678.1:p.Ser1037_Ala1038insGly...
ENST00000394412.8:c.2969_2989dup MANE Select ENSP00000377934.3:p.Ser996_Ala997insGlyGl...
ENST00000677187.1:n.643_663dup
ENST00000394412.7:c.2969_2989dup ENSP00000377934.3:p.Ser996_Ala997insGlyGl...
NM_198525.2:c.2969_2989dup NP_940927.2:p.Ser996_Ala997insGlyGlnLeuAr...
XM_005254902.2:c.2969_2989dup XP_005254959.1:p.Ser996_Ala997insGlyGlnLe...
XM_011521531.1:c.3092_3112dup XP_011519833.1:p.Ser1037_Ala1038insGlyGln...
XM_011521532.1:c.3089_3109dup XP_011519834.1:p.Ser1036_Ala1037insGlyGln...
XM_011521533.1:c.3089_3109dup XP_011519835.1:p.Ser1036_Ala1037insGlyGln...
XM_011521534.1:c.3092_3112dup XP_011519836.1:p.Ser1037_Ala1038insGlyGln...
XM_011521535.1:c.3092_3112dup XP_011519837.1:p.Ser1037_Ala1038insGlyGln...
XM_011521536.1:c.3092_3112dup XP_011519838.1:p.Ser1037_Ala1038insGlyGln...
XM_011521531.2:c.3092_3112dup XP_011519833.1:p.Ser1037_Ala1038insGlyGln...
NM_198525.3:c.2969_2989dup MANE Select NP_940927.2:p.Ser996_Ala997insGlyGlnLeuAr...