Canonical Allele Identifier: CA2627836329

Gene: KNL1

Linked Data

• gnomAD v4: 15-40611392-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611392C>T , CM000677.2:g.40611392C>T	GRCh38
NC_000015.9:g.40903590C>T , CM000677.1:g.40903590C>T	GRCh37
NC_000015.8:g.38690882C>T	NCBI36
NG_033114.1:g.22144C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.251-86C>T MANE Select	ENSP00000382576.3:n.251-86C>T
ENST00000346991.9:c.329-86C>T	ENSP00000335463.6:n.329-86C>T
ENST00000399668.6:c.251-86C>T	ENSP00000382576.2:n.251-86C>T
ENST00000527044.5:c.251-86C>T	ENSP00000432654.2:n.251-86C>T
ENST00000533001.1:n.396-86C>T
ENST00000534204.1:c.115+4960C>T	ENSP00000453857.1:n.115+4960C>T
ENST00000614337.4:n.626-92C>T
NM_144508.4:c.251-86C>T	NP_653091.3:n.251-86C>T
NM_170589.4:c.329-86C>T	NP_733468.3:n.329-86C>T
XM_011521817.1:c.251-86C>T	XP_011520119.1:n.251-86C>T
XM_017022432.1:c.-41+1095C>T	XP_016877921.1:n.-41+1095C>T
NM_144508.5:c.251-86C>T MANE Select	NP_653091.3:n.251-86C>T
NM_170589.5:c.329-86C>T	NP_733468.3:n.329-86C>T