Canonical Allele Identifier: CA2622629999

Gene: KL

Linked Data

• gnomAD v4: 13-33055429-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055429C>T , CM000675.2:g.33055429C>T	GRCh38
NC_000013.10:g.33629566C>T , CM000675.1:g.33629566C>T	GRCh37
NC_000013.9:g.32527566C>T	NCBI36
NG_011485.1:g.43996C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1599+114C>T MANE Select	ENSP00000369442.3:n.1599+114C>T
ENST00000380099.3:c.1599+114C>T	ENSP00000369442.3:n.1599+114C>T
ENST00000487852.1:n.1657+64C>T
NM_004795.3:c.1599+114C>T	NP_004786.2:n.1599+114C>T
XM_006719895.1:c.678+114C>T	XP_006719958.1:n.678+114C>T
XM_006719895.2:c.678+114C>T	XP_006719958.1:n.678+114C>T
NM_004795.4:c.1599+114C>T MANE Select	NP_004786.2:n.1599+114C>T