Canonical Allele Identifier: CA391773163

Gene: KNL1

Linked Data

• dbSNP Id: rs1893561889
• MyVariant Identifiers: chr15:g.40943673C>T (hg19) ; chr15:g.40651475C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651475C>T , CM000677.2:g.40651475C>T	GRCh38
NC_000015.9:g.40943673C>T , CM000677.1:g.40943673C>T	GRCh37
NC_000015.8:g.38730965C>T	NCBI36
NG_033114.1:g.62227C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6217C>T MANE Select	ENSP00000382576.3:p.Leu2073Phe
ENST00000346991.9:c.6295C>T	ENSP00000335463.6:p.Leu2099Phe
ENST00000399668.6:c.6217C>T	ENSP00000382576.2:p.Leu2073Phe
ENST00000526913.5:c.3350C>T
ENST00000532347.1:n.297C>T
NM_144508.4:c.6217C>T	NP_653091.3:p.Leu2073Phe
NM_170589.4:c.6295C>T	NP_733468.3:p.Leu2099Phe
XM_011521816.1:c.5893C>T	XP_011520118.1:p.Leu1965Phe
XM_011521817.1:c.6217C>T	XP_011520119.1:p.Leu2073Phe
XM_017022432.1:c.5893C>T	XP_016877921.1:p.Leu1965Phe
NM_144508.5:c.6217C>T MANE Select	NP_653091.3:p.Leu2073Phe
NM_170589.5:c.6295C>T	NP_733468.3:p.Leu2099Phe