Canonical Allele Identifier: CA387790564

Gene: KL

Linked Data

• gnomAD v4: 13-33053908-G-T
• MyVariant Identifiers: chr13:g.33628045G>T (hg19) ; chr13:g.33053908G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33053908G>T , CM000675.2:g.33053908G>T	GRCh38
NC_000013.10:g.33628045G>T , CM000675.1:g.33628045G>T	GRCh37
NC_000013.9:g.32526045G>T	NCBI36
NG_011485.1:g.42475G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380099.4:c.961G>T MANE Select	ENSP00000369442.3:p.Asp321Tyr
ENST00000380099.3:c.961G>T	ENSP00000369442.3:p.Asp321Tyr
ENST00000487852.1:n.969G>T
NM_004795.3:c.961G>T	NP_004786.2:p.Asp321Tyr
XM_006719895.1:c.40G>T	XP_006719958.1:p.Asp14Tyr
XM_006719895.2:c.40G>T	XP_006719958.1:p.Asp14Tyr
NM_004795.4:c.961G>T MANE Select	NP_004786.2:p.Asp321Tyr