Canonical Allele Identifier: CA391732386

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40914002C>T (hg19) ; chr15:g.40621804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621804C>T , CM000677.2:g.40621804C>T	GRCh38
NC_000015.9:g.40914002C>T , CM000677.1:g.40914002C>T	GRCh37
NC_000015.8:g.38701294C>T	NCBI36
NG_033114.1:g.32556C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1540C>T MANE Select	ENSP00000382576.3:p.Pro514Ser
ENST00000346991.9:c.1618C>T	ENSP00000335463.6:p.Pro540Ser
ENST00000399668.6:c.1540C>T	ENSP00000382576.2:p.Pro514Ser
ENST00000527044.5:c.1540C>T	ENSP00000432654.2:p.Pro514Ser
ENST00000533001.1:n.1685C>T
ENST00000534204.1:c.116-7520C>T	ENSP00000453857.1:n.116-7520C>T
ENST00000614337.4:n.1856C>T
NM_144508.4:c.1540C>T	NP_653091.3:p.Pro514Ser
NM_170589.4:c.1618C>T	NP_733468.3:p.Pro540Ser
XM_011521816.1:c.1216C>T	XP_011520118.1:p.Pro406Ser
XM_011521817.1:c.1540C>T	XP_011520119.1:p.Pro514Ser
XM_017022432.1:c.1216C>T	XP_016877921.1:p.Pro406Ser
NM_144508.5:c.1540C>T MANE Select	NP_653091.3:p.Pro514Ser
NM_170589.5:c.1618C>T	NP_733468.3:p.Pro540Ser