Canonical Allele Identifier: CA376896168

Gene: KIFBP

Linked Data

• gnomAD v4: 10-69005083-T-C
• MyVariant Identifiers: chr10:g.70764839T>C (hg19) ; chr10:g.69005083T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005083T>C , CM000672.2:g.69005083T>C	GRCh38
NC_000010.10:g.70764839T>C , CM000672.1:g.70764839T>C	GRCh37
NC_000010.9:g.70434845T>C	NCBI36
NG_017061.1:g.21363T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.563T>C MANE Select	ENSP00000354848.4:p.Leu188Pro
ENST00000625461.2:n.593T>C
ENST00000626493.2:c.563T>C	ENSP00000486692.1:p.Leu188Pro
ENST00000635779.2:c.563T>C	ENSP00000489663.1:p.Leu188Pro
ENST00000635971.2:c.563T>C	ENSP00000489878.2:p.Leu188Pro
ENST00000636200.2:c.563T>C	ENSP00000490113.2:p.Leu188Pro
ENST00000637101.2:c.*136T>C	ENSP00000490704.1:n.*136T>C
ENST00000637104.2:c.*132T>C	ENSP00000490019.2:n.*132T>C
ENST00000637323.2:c.*204T>C	ENSP00000489659.2:n.*204T>C
ENST00000637420.2:c.563T>C	ENSP00000490404.2:p.Leu188Pro
ENST00000637738.2:c.563T>C	ENSP00000490742.2:p.Leu188Pro
ENST00000638119.2:c.638T>C	ENSP00000490026.1:p.Leu213Pro
ENST00000674660.1:c.526-14T>C	ENSP00000502562.1:n.526-14T>C
ENST00000674688.1:n.593T>C
ENST00000674897.1:c.47T>C	ENSP00000502225.1:p.Leu16Pro
ENST00000674936.1:c.563T>C	ENSP00000502484.1:p.Leu188Pro
ENST00000675576.1:c.464T>C	ENSP00000502750.1:p.Leu155Pro
ENST00000676080.1:c.*76T>C	ENSP00000502706.1:n.*76T>C
ENST00000361983.6:c.563T>C	ENSP00000354848.4:p.Leu188Pro
ENST00000625461.1:n.279T>C
ENST00000626493.1:c.563T>C	ENSP00000486692.1:p.Leu188Pro
NM_015634.3:c.563T>C	NP_056449.1:p.Leu188Pro
NM_015634.4:c.563T>C MANE Select	NP_056449.1:p.Leu188Pro