Canonical Allele Identifier: CA391731448

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40913858C>T (hg19) ; chr15:g.40621660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621660C>T , CM000677.2:g.40621660C>T	GRCh38
NC_000015.9:g.40913858C>T , CM000677.1:g.40913858C>T	GRCh37
NC_000015.8:g.38701150C>T	NCBI36
NG_033114.1:g.32412C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1396C>T MANE Select	ENSP00000382576.3:p.Pro466Ser
ENST00000346991.9:c.1474C>T	ENSP00000335463.6:p.Pro492Ser
ENST00000399668.6:c.1396C>T	ENSP00000382576.2:p.Pro466Ser
ENST00000527044.5:c.1396C>T	ENSP00000432654.2:p.Pro466Ser
ENST00000533001.1:n.1541C>T
ENST00000534204.1:c.116-7664C>T	ENSP00000453857.1:n.116-7664C>T
ENST00000614337.4:n.1712C>T
NM_144508.4:c.1396C>T	NP_653091.3:p.Pro466Ser
NM_170589.4:c.1474C>T	NP_733468.3:p.Pro492Ser
XM_011521816.1:c.1072C>T	XP_011520118.1:p.Pro358Ser
XM_011521817.1:c.1396C>T	XP_011520119.1:p.Pro466Ser
XM_017022432.1:c.1072C>T	XP_016877921.1:p.Pro358Ser
NM_144508.5:c.1396C>T MANE Select	NP_653091.3:p.Pro466Ser
NM_170589.5:c.1474C>T	NP_733468.3:p.Pro492Ser