Canonical Allele Identifier: CA376896340

Gene: KIFBP

Linked Data

• MyVariant Identifiers: chr10:g.70764872G>C (hg19) ; chr10:g.69005116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005116G>C , CM000672.2:g.69005116G>C	GRCh38
NC_000010.10:g.70764872G>C , CM000672.1:g.70764872G>C	GRCh37
NC_000010.9:g.70434878G>C	NCBI36
NG_017061.1:g.21396G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.596G>C MANE Select	ENSP00000354848.4:p.Arg199Thr
ENST00000625461.2:n.626G>C
ENST00000626493.2:c.596G>C	ENSP00000486692.1:p.Arg199Thr
ENST00000635779.2:c.596G>C	ENSP00000489663.1:p.Arg199Thr
ENST00000635971.2:c.596G>C	ENSP00000489878.2:p.Arg199Thr
ENST00000636200.2:c.596G>C	ENSP00000490113.2:p.Arg199Thr
ENST00000637101.2:c.*169G>C	ENSP00000490704.1:n.*169G>C
ENST00000637104.2:c.*165G>C	ENSP00000490019.2:n.*165G>C
ENST00000637323.2:c.*237G>C	ENSP00000489659.2:n.*237G>C
ENST00000637420.2:c.596G>C	ENSP00000490404.2:p.Arg199Thr
ENST00000637738.2:c.596G>C	ENSP00000490742.2:p.Arg199Thr
ENST00000638119.2:c.671G>C	ENSP00000490026.1:p.Arg224Thr
ENST00000674660.1:c.545G>C	ENSP00000502562.1:p.Arg182Thr
ENST00000674688.1:n.626G>C
ENST00000674897.1:c.80G>C	ENSP00000502225.1:p.Arg27Thr
ENST00000674936.1:c.596G>C	ENSP00000502484.1:p.Arg199Thr
ENST00000675576.1:c.497G>C	ENSP00000502750.1:p.Arg166Thr
ENST00000676080.1:c.*109G>C	ENSP00000502706.1:n.*109G>C
ENST00000361983.6:c.596G>C	ENSP00000354848.4:p.Arg199Thr
ENST00000625461.1:n.312G>C
ENST00000626493.1:c.596G>C	ENSP00000486692.1:p.Arg199Thr
NM_015634.3:c.596G>C	NP_056449.1:p.Arg199Thr
NM_015634.4:c.596G>C MANE Select	NP_056449.1:p.Arg199Thr