Canonical Allele Identifier: CA489772926

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943669A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651471A>G , CM000677.2:g.40651471A>G	GRCh38
NC_000015.9:g.40943669A>G , CM000677.1:g.40943669A>G	GRCh37
NC_000015.8:g.38730961A>G	NCBI36
NG_033114.1:g.62223A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6213A>G MANE Select	ENSP00000382576.3:p.Arg2071=
ENST00000346991.9:c.6291A>G	ENSP00000335463.6:p.Arg2097=
ENST00000399668.6:c.6213A>G	ENSP00000382576.2:p.Arg2071=
ENST00000526913.5:c.3346A>G
ENST00000532347.1:n.293A>G
NM_144508.4:c.6213A>G	NP_653091.3:p.Arg2071=
NM_170589.4:c.6291A>G	NP_733468.3:p.Arg2097=
XM_011521816.1:c.5889A>G	XP_011520118.1:p.Arg1963=
XM_011521817.1:c.6213A>G	XP_011520119.1:p.Arg2071=
XM_017022432.1:c.5889A>G	XP_016877921.1:p.Arg1963=
NM_144508.5:c.6213A>G MANE Select	NP_653091.3:p.Arg2071=
NM_170589.5:c.6291A>G	NP_733468.3:p.Arg2097=