Canonical Allele Identifier: CA391773592

Gene: KNL1

Linked Data

• dbSNP Id: rs1413725715
• MyVariant Identifiers: chr15:g.40943764A>G (hg19) ; chr15:g.40651566A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651566A>G , CM000677.2:g.40651566A>G	GRCh38
NC_000015.9:g.40943764A>G , CM000677.1:g.40943764A>G	GRCh37
NC_000015.8:g.38731056A>G	NCBI36
NG_033114.1:g.62318A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6308A>G MANE Select	ENSP00000382576.3:p.Gln2103Arg
ENST00000346991.9:c.6386A>G	ENSP00000335463.6:p.Gln2129Arg
ENST00000399668.6:c.6308A>G	ENSP00000382576.2:p.Gln2103Arg
ENST00000526913.5:c.3441A>G
ENST00000532347.1:n.388A>G
NM_144508.4:c.6308A>G	NP_653091.3:p.Gln2103Arg
NM_170589.4:c.6386A>G	NP_733468.3:p.Gln2129Arg
XM_011521816.1:c.5984A>G	XP_011520118.1:p.Gln1995Arg
XM_011521817.1:c.6308A>G	XP_011520119.1:p.Gln2103Arg
XM_017022432.1:c.5984A>G	XP_016877921.1:p.Gln1995Arg
NM_144508.5:c.6308A>G MANE Select	NP_653091.3:p.Gln2103Arg
NM_170589.5:c.6386A>G	NP_733468.3:p.Gln2129Arg