Canonical Allele Identifier: CA470008557
Gene: KIFBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.70764837T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005081T>C , CM000672.2:g.69005081T>C GRCh38
NC_000010.10:g.70764837T>C , CM000672.1:g.70764837T>C GRCh37
NC_000010.9:g.70434843T>C NCBI36
NG_017061.1:g.21361T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.561T>C MANE Select ENSP00000354848.4:p.Phe187=
ENST00000625461.2:n.591T>C
ENST00000626493.2:c.561T>C ENSP00000486692.1:p.Phe187=
ENST00000635779.2:c.561T>C ENSP00000489663.1:p.Phe187=
ENST00000635971.2:c.561T>C ENSP00000489878.2:p.Phe187=
ENST00000636200.2:c.561T>C ENSP00000490113.2:p.Phe187=
ENST00000637101.2:c.*134T>C ENSP00000490704.1:n.*134T>C
ENST00000637104.2:c.*130T>C ENSP00000490019.2:n.*130T>C
ENST00000637323.2:c.*202T>C ENSP00000489659.2:n.*202T>C
ENST00000637420.2:c.561T>C ENSP00000490404.2:p.Phe187=
ENST00000637738.2:c.561T>C ENSP00000490742.2:p.Phe187=
ENST00000638119.2:c.636T>C ENSP00000490026.1:p.Phe212=
ENST00000674660.1:c.526-16T>C ENSP00000502562.1:n.526-16T>C
ENST00000674688.1:n.591T>C
ENST00000674897.1:c.45T>C ENSP00000502225.1:p.Phe15=
ENST00000674936.1:c.561T>C ENSP00000502484.1:p.Phe187=
ENST00000675576.1:c.462T>C ENSP00000502750.1:p.Phe154=
ENST00000676080.1:c.*74T>C ENSP00000502706.1:n.*74T>C
ENST00000361983.6:c.561T>C ENSP00000354848.4:p.Phe187=
ENST00000625461.1:n.277T>C
ENST00000626493.1:c.561T>C ENSP00000486692.1:p.Phe187=
NM_015634.3:c.561T>C NP_056449.1:p.Phe187=
NM_015634.4:c.561T>C MANE Select NP_056449.1:p.Phe187=