Canonical Allele Identifier: CA391773431

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943729A>T (hg19) ; chr15:g.40651531A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651531A>T , CM000677.2:g.40651531A>T	GRCh38
NC_000015.9:g.40943729A>T , CM000677.1:g.40943729A>T	GRCh37
NC_000015.8:g.38731021A>T	NCBI36
NG_033114.1:g.62283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6273A>T MANE Select	ENSP00000382576.3:p.Gln2091His
ENST00000346991.9:c.6351A>T	ENSP00000335463.6:p.Gln2117His
ENST00000399668.6:c.6273A>T	ENSP00000382576.2:p.Gln2091His
ENST00000526913.5:c.3406A>T
ENST00000532347.1:n.353A>T
NM_144508.4:c.6273A>T	NP_653091.3:p.Gln2091His
NM_170589.4:c.6351A>T	NP_733468.3:p.Gln2117His
XM_011521816.1:c.5949A>T	XP_011520118.1:p.Gln1983His
XM_011521817.1:c.6273A>T	XP_011520119.1:p.Gln2091His
XM_017022432.1:c.5949A>T	XP_016877921.1:p.Gln1983His
NM_144508.5:c.6273A>T MANE Select	NP_653091.3:p.Gln2091His
NM_170589.5:c.6351A>T	NP_733468.3:p.Gln2117His