Canonical Allele Identifier: CA489772942

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943676T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651478T>C , CM000677.2:g.40651478T>C	GRCh38
NC_000015.9:g.40943676T>C , CM000677.1:g.40943676T>C	GRCh37
NC_000015.8:g.38730968T>C	NCBI36
NG_033114.1:g.62230T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6220T>C MANE Select	ENSP00000382576.3:p.Leu2074=
ENST00000346991.9:c.6298T>C	ENSP00000335463.6:p.Leu2100=
ENST00000399668.6:c.6220T>C	ENSP00000382576.2:p.Leu2074=
ENST00000526913.5:c.3353T>C
ENST00000532347.1:n.300T>C
NM_144508.4:c.6220T>C	NP_653091.3:p.Leu2074=
NM_170589.4:c.6298T>C	NP_733468.3:p.Leu2100=
XM_011521816.1:c.5896T>C	XP_011520118.1:p.Leu1966=
XM_011521817.1:c.6220T>C	XP_011520119.1:p.Leu2074=
XM_017022432.1:c.5896T>C	XP_016877921.1:p.Leu1966=
NM_144508.5:c.6220T>C MANE Select	NP_653091.3:p.Leu2074=
NM_170589.5:c.6298T>C	NP_733468.3:p.Leu2100=