Canonical Allele Identifier: CA483442381

Gene: KL

Linked Data

• MyVariant Identifiers: chr13:g.33629395C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33055258C>T , CM000675.2:g.33055258C>T	GRCh38
NC_000013.10:g.33629395C>T , CM000675.1:g.33629395C>T	GRCh37
NC_000013.9:g.32527395C>T	NCBI36
NG_011485.1:g.43825C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.1542C>T MANE Select	ENSP00000369442.3:p.Pro514=
ENST00000380099.3:c.1542C>T	ENSP00000369442.3:p.Pro514=
ENST00000487852.1:n.1550C>T
NM_004795.3:c.1542C>T	NP_004786.2:p.Pro514=
XM_006719895.1:c.621C>T	XP_006719958.1:p.Pro207=
XM_006719895.2:c.621C>T	XP_006719958.1:p.Pro207=
NM_004795.4:c.1542C>T MANE Select	NP_004786.2:p.Pro514=