Canonical Allele Identifier: CA391773149

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651469-A-G
• MyVariant Identifiers: chr15:g.40943667A>G (hg19) ; chr15:g.40651469A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651469A>G , CM000677.2:g.40651469A>G	GRCh38
NC_000015.9:g.40943667A>G , CM000677.1:g.40943667A>G	GRCh37
NC_000015.8:g.38730959A>G	NCBI36
NG_033114.1:g.62221A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6213-2A>G MANE Select	ENSP00000382576.3:n.6213-2A>G
ENST00000346991.9:c.6291-2A>G	ENSP00000335463.6:n.6291-2A>G
ENST00000399668.6:c.6213-2A>G	ENSP00000382576.2:n.6213-2A>G
ENST00000526913.5:c.3346-2A>G
ENST00000532347.1:n.293-2A>G
NM_144508.4:c.6213-2A>G	NP_653091.3:n.6213-2A>G
NM_170589.4:c.6291-2A>G	NP_733468.3:n.6291-2A>G
XM_011521816.1:c.5889-2A>G	XP_011520118.1:n.5889-2A>G
XM_011521817.1:c.6213-2A>G	XP_011520119.1:n.6213-2A>G
XM_017022432.1:c.5889-2A>G	XP_016877921.1:n.5889-2A>G
NM_144508.5:c.6213-2A>G MANE Select	NP_653091.3:n.6213-2A>G
NM_170589.5:c.6291-2A>G	NP_733468.3:n.6291-2A>G