Canonical Allele Identifier: CA489977060

Gene: KNL1

Linked Data

• dbSNP Id: rs1215147892
• gnomAD v2: 15-40913743-T-C
• gnomAD v3: 15-40621545-T-C
• gnomAD v4: 15-40621545-T-C
• MyVariant Identifiers: chr15:g.40913743T>C (hg19) ; chr15:g.40621545T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621545T>C , CM000677.2:g.40621545T>C	GRCh38
NC_000015.9:g.40913743T>C , CM000677.1:g.40913743T>C	GRCh37
NC_000015.8:g.38701035T>C	NCBI36
NG_033114.1:g.32297T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.1281T>C MANE Select	ENSP00000382576.3:p.Thr427=
ENST00000346991.9:c.1359T>C	ENSP00000335463.6:p.Thr453=
ENST00000399668.6:c.1281T>C	ENSP00000382576.2:p.Thr427=
ENST00000527044.5:c.1281T>C	ENSP00000432654.2:p.Thr427=
ENST00000533001.1:n.1426T>C
ENST00000534204.1:c.116-7779T>C	ENSP00000453857.1:n.116-7779T>C
ENST00000614337.4:n.1597T>C
NM_144508.4:c.1281T>C	NP_653091.3:p.Thr427=
NM_170589.4:c.1359T>C	NP_733468.3:p.Thr453=
XM_011521816.1:c.957T>C	XP_011520118.1:p.Thr319=
XM_011521817.1:c.1281T>C	XP_011520119.1:p.Thr427=
XM_017022432.1:c.957T>C	XP_016877921.1:p.Thr319=
NM_144508.5:c.1281T>C MANE Select	NP_653091.3:p.Thr427=
NM_170589.5:c.1359T>C	NP_733468.3:p.Thr453=