Canonical Allele Identifier: CA489772934

Gene: KNL1

Linked Data

• dbSNP Id: rs1397115546
• gnomAD v2: 15-40943672-T-C
• gnomAD v3: 15-40651474-T-C
• gnomAD v4: 15-40651474-T-C
• MyVariant Identifiers: chr15:g.40943672T>C (hg19) ; chr15:g.40651474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651474T>C , CM000677.2:g.40651474T>C	GRCh38
NC_000015.9:g.40943672T>C , CM000677.1:g.40943672T>C	GRCh37
NC_000015.8:g.38730964T>C	NCBI36
NG_033114.1:g.62226T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6216T>C MANE Select	ENSP00000382576.3:p.Asn2072=
ENST00000346991.9:c.6294T>C	ENSP00000335463.6:p.Asn2098=
ENST00000399668.6:c.6216T>C	ENSP00000382576.2:p.Asn2072=
ENST00000526913.5:c.3349T>C
ENST00000532347.1:n.296T>C
NM_144508.4:c.6216T>C	NP_653091.3:p.Asn2072=
NM_170589.4:c.6294T>C	NP_733468.3:p.Asn2098=
XM_011521816.1:c.5892T>C	XP_011520118.1:p.Asn1964=
XM_011521817.1:c.6216T>C	XP_011520119.1:p.Asn2072=
XM_017022432.1:c.5892T>C	XP_016877921.1:p.Asn1964=
NM_144508.5:c.6216T>C MANE Select	NP_653091.3:p.Asn2072=
NM_170589.5:c.6294T>C	NP_733468.3:p.Asn2098=