Canonical Allele Identifier: CA391730537

Gene: KNL1

Linked Data

• dbSNP Id: rs1892528392
• MyVariant Identifiers: chr15:g.40913744G>C (hg19) ; chr15:g.40621546G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621546G>C , CM000677.2:g.40621546G>C	GRCh38
NC_000015.9:g.40913744G>C , CM000677.1:g.40913744G>C	GRCh37
NC_000015.8:g.38701036G>C	NCBI36
NG_033114.1:g.32298G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.1282G>C MANE Select	ENSP00000382576.3:p.Val428Leu
ENST00000346991.9:c.1360G>C	ENSP00000335463.6:p.Val454Leu
ENST00000399668.6:c.1282G>C	ENSP00000382576.2:p.Val428Leu
ENST00000527044.5:c.1282G>C	ENSP00000432654.2:p.Val428Leu
ENST00000533001.1:n.1427G>C
ENST00000534204.1:c.116-7778G>C	ENSP00000453857.1:n.116-7778G>C
ENST00000614337.4:n.1598G>C
NM_144508.4:c.1282G>C	NP_653091.3:p.Val428Leu
NM_170589.4:c.1360G>C	NP_733468.3:p.Val454Leu
XM_011521816.1:c.958G>C	XP_011520118.1:p.Val320Leu
XM_011521817.1:c.1282G>C	XP_011520119.1:p.Val428Leu
XM_017022432.1:c.958G>C	XP_016877921.1:p.Val320Leu
NM_144508.5:c.1282G>C MANE Select	NP_653091.3:p.Val428Leu
NM_170589.5:c.1360G>C	NP_733468.3:p.Val454Leu