Canonical Allele Identifier: CA470008597

Gene: KIFBP

Linked Data

• MyVariant Identifiers: chr10:g.70764843T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005087T>G , CM000672.2:g.69005087T>G	GRCh38
NC_000010.10:g.70764843T>G , CM000672.1:g.70764843T>G	GRCh37
NC_000010.9:g.70434849T>G	NCBI36
NG_017061.1:g.21367T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.567T>G MANE Select	ENSP00000354848.4:p.Pro189=
ENST00000625461.2:n.597T>G
ENST00000626493.2:c.567T>G	ENSP00000486692.1:p.Pro189=
ENST00000635779.2:c.567T>G	ENSP00000489663.1:p.Pro189=
ENST00000635971.2:c.567T>G	ENSP00000489878.2:p.Pro189=
ENST00000636200.2:c.567T>G	ENSP00000490113.2:p.Pro189=
ENST00000637101.2:c.*140T>G	ENSP00000490704.1:n.*140T>G
ENST00000637104.2:c.*136T>G	ENSP00000490019.2:n.*136T>G
ENST00000637323.2:c.*208T>G	ENSP00000489659.2:n.*208T>G
ENST00000637420.2:c.567T>G	ENSP00000490404.2:p.Pro189=
ENST00000637738.2:c.567T>G	ENSP00000490742.2:p.Pro189=
ENST00000638119.2:c.642T>G	ENSP00000490026.1:p.Pro214=
ENST00000674660.1:c.526-10T>G	ENSP00000502562.1:n.526-10T>G
ENST00000674688.1:n.597T>G
ENST00000674897.1:c.51T>G	ENSP00000502225.1:p.Pro17=
ENST00000674936.1:c.567T>G	ENSP00000502484.1:p.Pro189=
ENST00000675576.1:c.468T>G	ENSP00000502750.1:p.Pro156=
ENST00000676080.1:c.*80T>G	ENSP00000502706.1:n.*80T>G
ENST00000361983.6:c.567T>G	ENSP00000354848.4:p.Pro189=
ENST00000625461.1:n.283T>G
ENST00000626493.1:c.567T>G	ENSP00000486692.1:p.Pro189=
NM_015634.3:c.567T>G	NP_056449.1:p.Pro189=
NM_015634.4:c.567T>G MANE Select	NP_056449.1:p.Pro189=