Canonical Allele Identifier: CA376896338

Gene: KIFBP

Linked Data

• MyVariant Identifiers: chr10:g.70764871A>T (hg19) ; chr10:g.69005115A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005115A>T , CM000672.2:g.69005115A>T	GRCh38
NC_000010.10:g.70764871A>T , CM000672.1:g.70764871A>T	GRCh37
NC_000010.9:g.70434877A>T	NCBI36
NG_017061.1:g.21395A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.595A>T MANE Select	ENSP00000354848.4:p.Arg199Ter
ENST00000625461.2:n.625A>T
ENST00000626493.2:c.595A>T	ENSP00000486692.1:p.Arg199Ter
ENST00000635779.2:c.595A>T	ENSP00000489663.1:p.Arg199Ter
ENST00000635971.2:c.595A>T	ENSP00000489878.2:p.Arg199Ter
ENST00000636200.2:c.595A>T	ENSP00000490113.2:p.Arg199Ter
ENST00000637101.2:c.*168A>T	ENSP00000490704.1:n.*168A>T
ENST00000637104.2:c.*164A>T	ENSP00000490019.2:n.*164A>T
ENST00000637323.2:c.*236A>T	ENSP00000489659.2:n.*236A>T
ENST00000637420.2:c.595A>T	ENSP00000490404.2:p.Arg199Ter
ENST00000637738.2:c.595A>T	ENSP00000490742.2:p.Arg199Ter
ENST00000638119.2:c.670A>T	ENSP00000490026.1:p.Arg224Ter
ENST00000674660.1:c.544A>T	ENSP00000502562.1:p.Arg182Ter
ENST00000674688.1:n.625A>T
ENST00000674897.1:c.79A>T	ENSP00000502225.1:p.Arg27Ter
ENST00000674936.1:c.595A>T	ENSP00000502484.1:p.Arg199Ter
ENST00000675576.1:c.496A>T	ENSP00000502750.1:p.Arg166Ter
ENST00000676080.1:c.*108A>T	ENSP00000502706.1:n.*108A>T
ENST00000361983.6:c.595A>T	ENSP00000354848.4:p.Arg199Ter
ENST00000625461.1:n.311A>T
ENST00000626493.1:c.595A>T	ENSP00000486692.1:p.Arg199Ter
NM_015634.3:c.595A>T	NP_056449.1:p.Arg199Ter
NM_015634.4:c.595A>T MANE Select	NP_056449.1:p.Arg199Ter