Canonical Allele Identifier: CA489772941

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651477-C-T
• MyVariant Identifiers: chr15:g.40943675C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651477C>T , CM000677.2:g.40651477C>T	GRCh38
NC_000015.9:g.40943675C>T , CM000677.1:g.40943675C>T	GRCh37
NC_000015.8:g.38730967C>T	NCBI36
NG_033114.1:g.62229C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6219C>T MANE Select	ENSP00000382576.3:p.Leu2073=
ENST00000346991.9:c.6297C>T	ENSP00000335463.6:p.Leu2099=
ENST00000399668.6:c.6219C>T	ENSP00000382576.2:p.Leu2073=
ENST00000526913.5:c.3352C>T
ENST00000532347.1:n.299C>T
NM_144508.4:c.6219C>T	NP_653091.3:p.Leu2073=
NM_170589.4:c.6297C>T	NP_733468.3:p.Leu2099=
XM_011521816.1:c.5895C>T	XP_011520118.1:p.Leu1965=
XM_011521817.1:c.6219C>T	XP_011520119.1:p.Leu2073=
XM_017022432.1:c.5895C>T	XP_016877921.1:p.Leu1965=
NM_144508.5:c.6219C>T MANE Select	NP_653091.3:p.Leu2073=
NM_170589.5:c.6297C>T	NP_733468.3:p.Leu2099=