Canonical Allele Identifier: CA391773162

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943673C>G (hg19) ; chr15:g.40651475C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6217C>G MANE Select	ENSP00000382576.3:p.Leu2073Val
ENST00000346991.9:c.6295C>G	ENSP00000335463.6:p.Leu2099Val
ENST00000399668.6:c.6217C>G	ENSP00000382576.2:p.Leu2073Val
ENST00000526913.5:c.3350C>G
ENST00000532347.1:n.297C>G
NM_144508.4:c.6217C>G	NP_653091.3:p.Leu2073Val
NM_170589.4:c.6295C>G	NP_733468.3:p.Leu2099Val
XM_011521816.1:c.5893C>G	XP_011520118.1:p.Leu1965Val
XM_011521817.1:c.6217C>G	XP_011520119.1:p.Leu2073Val
XM_017022432.1:c.5893C>G	XP_016877921.1:p.Leu1965Val
NM_144508.5:c.6217C>G MANE Select	NP_653091.3:p.Leu2073Val
NM_170589.5:c.6295C>G	NP_733468.3:p.Leu2099Val