Canonical Allele Identifier: CA391773159

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943671A>T (hg19) ; chr15:g.40651473A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651473A>T , CM000677.2:g.40651473A>T	GRCh38
NC_000015.9:g.40943671A>T , CM000677.1:g.40943671A>T	GRCh37
NC_000015.8:g.38730963A>T	NCBI36
NG_033114.1:g.62225A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6215A>T MANE Select	ENSP00000382576.3:p.Asn2072Ile
ENST00000346991.9:c.6293A>T	ENSP00000335463.6:p.Asn2098Ile
ENST00000399668.6:c.6215A>T	ENSP00000382576.2:p.Asn2072Ile
ENST00000526913.5:c.3348A>T
ENST00000532347.1:n.295A>T
NM_144508.4:c.6215A>T	NP_653091.3:p.Asn2072Ile
NM_170589.4:c.6293A>T	NP_733468.3:p.Asn2098Ile
XM_011521816.1:c.5891A>T	XP_011520118.1:p.Asn1964Ile
XM_011521817.1:c.6215A>T	XP_011520119.1:p.Asn2072Ile
XM_017022432.1:c.5891A>T	XP_016877921.1:p.Asn1964Ile
NM_144508.5:c.6215A>T MANE Select	NP_653091.3:p.Asn2072Ile
NM_170589.5:c.6293A>T	NP_733468.3:p.Asn2098Ile