Canonical Allele Identifier: CA391773485

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943739A>T (hg19) ; chr15:g.40651541A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651541A>T , CM000677.2:g.40651541A>T	GRCh38
NC_000015.9:g.40943739A>T , CM000677.1:g.40943739A>T	GRCh37
NC_000015.8:g.38731031A>T	NCBI36
NG_033114.1:g.62293A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6283A>T MANE Select	ENSP00000382576.3:p.Asn2095Tyr
ENST00000346991.9:c.6361A>T	ENSP00000335463.6:p.Asn2121Tyr
ENST00000399668.6:c.6283A>T	ENSP00000382576.2:p.Asn2095Tyr
ENST00000526913.5:c.3416A>T
ENST00000532347.1:n.363A>T
NM_144508.4:c.6283A>T	NP_653091.3:p.Asn2095Tyr
NM_170589.4:c.6361A>T	NP_733468.3:p.Asn2121Tyr
XM_011521816.1:c.5959A>T	XP_011520118.1:p.Asn1987Tyr
XM_011521817.1:c.6283A>T	XP_011520119.1:p.Asn2095Tyr
XM_017022432.1:c.5959A>T	XP_016877921.1:p.Asn1987Tyr
NM_144508.5:c.6283A>T MANE Select	NP_653091.3:p.Asn2095Tyr
NM_170589.5:c.6361A>T	NP_733468.3:p.Asn2121Tyr