Canonical Allele Identifier: CA376896112

Gene: KIFBP

Linked Data

• MyVariant Identifiers: chr10:g.70764827C>A (hg19) ; chr10:g.69005071C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005071C>A , CM000672.2:g.69005071C>A	GRCh38
NC_000010.10:g.70764827C>A , CM000672.1:g.70764827C>A	GRCh37
NC_000010.9:g.70434833C>A	NCBI36
NG_017061.1:g.21351C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.551C>A MANE Select	ENSP00000354848.4:p.Thr184Asn
ENST00000625461.2:n.581C>A
ENST00000626493.2:c.551C>A	ENSP00000486692.1:p.Thr184Asn
ENST00000635779.2:c.551C>A	ENSP00000489663.1:p.Thr184Asn
ENST00000635971.2:c.551C>A	ENSP00000489878.2:p.Thr184Asn
ENST00000636200.2:c.551C>A	ENSP00000490113.2:p.Thr184Asn
ENST00000637101.2:c.*124C>A	ENSP00000490704.1:n.*124C>A
ENST00000637104.2:c.*120C>A	ENSP00000490019.2:n.*120C>A
ENST00000637323.2:c.*192C>A	ENSP00000489659.2:n.*192C>A
ENST00000637420.2:c.551C>A	ENSP00000490404.2:p.Thr184Asn
ENST00000637738.2:c.551C>A	ENSP00000490742.2:p.Thr184Asn
ENST00000638119.2:c.626C>A	ENSP00000490026.1:p.Thr209Asn
ENST00000674660.1:c.526-26C>A	ENSP00000502562.1:n.526-26C>A
ENST00000674688.1:n.581C>A
ENST00000674897.1:c.35C>A	ENSP00000502225.1:p.Thr12Asn
ENST00000674936.1:c.551C>A	ENSP00000502484.1:p.Thr184Asn
ENST00000675576.1:c.452C>A	ENSP00000502750.1:p.Thr151Asn
ENST00000676080.1:c.*64C>A	ENSP00000502706.1:n.*64C>A
ENST00000361983.6:c.551C>A	ENSP00000354848.4:p.Thr184Asn
ENST00000625461.1:n.267C>A
ENST00000626493.1:c.551C>A	ENSP00000486692.1:p.Thr184Asn
NM_015634.3:c.551C>A	NP_056449.1:p.Thr184Asn
NM_015634.4:c.551C>A MANE Select	NP_056449.1:p.Thr184Asn