Canonical Allele Identifier: CA391773177

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943679G>C (hg19) ; chr15:g.40651481G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651481G>C , CM000677.2:g.40651481G>C	GRCh38
NC_000015.9:g.40943679G>C , CM000677.1:g.40943679G>C	GRCh37
NC_000015.8:g.38730971G>C	NCBI36
NG_033114.1:g.62233G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6223G>C MANE Select	ENSP00000382576.3:p.Glu2075Gln
ENST00000346991.9:c.6301G>C	ENSP00000335463.6:p.Glu2101Gln
ENST00000399668.6:c.6223G>C	ENSP00000382576.2:p.Glu2075Gln
ENST00000526913.5:c.3356G>C
ENST00000532347.1:n.303G>C
NM_144508.4:c.6223G>C	NP_653091.3:p.Glu2075Gln
NM_170589.4:c.6301G>C	NP_733468.3:p.Glu2101Gln
XM_011521816.1:c.5899G>C	XP_011520118.1:p.Glu1967Gln
XM_011521817.1:c.6223G>C	XP_011520119.1:p.Glu2075Gln
XM_017022432.1:c.5899G>C	XP_016877921.1:p.Glu1967Gln
NM_144508.5:c.6223G>C MANE Select	NP_653091.3:p.Glu2075Gln
NM_170589.5:c.6301G>C	NP_733468.3:p.Glu2101Gln