Canonical Allele Identifier: CA391773158

Gene: KNL1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6215A>C MANE Select	ENSP00000382576.3:p.Asn2072Thr
ENST00000346991.9:c.6293A>C	ENSP00000335463.6:p.Asn2098Thr
ENST00000399668.6:c.6215A>C	ENSP00000382576.2:p.Asn2072Thr
ENST00000526913.5:c.3348A>C
ENST00000532347.1:n.295A>C
NM_144508.4:c.6215A>C	NP_653091.3:p.Asn2072Thr
NM_170589.4:c.6293A>C	NP_733468.3:p.Asn2098Thr
XM_011521816.1:c.5891A>C	XP_011520118.1:p.Asn1964Thr
XM_011521817.1:c.6215A>C	XP_011520119.1:p.Asn2072Thr
XM_017022432.1:c.5891A>C	XP_016877921.1:p.Asn1964Thr
NM_144508.5:c.6215A>C MANE Select	NP_653091.3:p.Asn2072Thr
NM_170589.5:c.6293A>C	NP_733468.3:p.Asn2098Thr