Canonical Allele Identifier: CA2627840307

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651466-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651466T>C , CM000677.2:g.40651466T>C	GRCh38
NC_000015.9:g.40943664T>C , CM000677.1:g.40943664T>C	GRCh37
NC_000015.8:g.38730956T>C	NCBI36
NG_033114.1:g.62218T>C

Transcript Alleles

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