Canonical Allele Identifier: CA1028158389
Gene: MATN3 HGNC NCBI
WDR35-DT HGNC NCBI

Linked Data

dbSNP Id: rs1672916764

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19998223del , CM000664.2:g.19998223del GRCh38
NC_000002.11:g.20197984del , CM000664.1:g.20197984del GRCh37
NC_000002.10:g.20061465del NCBI36
NG_008087.1:g.19472del

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.1169-964del (MATN3) MANE Select ENSP00000383894.3:n.1169-964del
ENST00000407540.7:c.1169-964del (MATN3) ENSP00000383894.3:n.1169-964del
ENST00000421259.2:c.1043-964del (MATN3) ENSP00000398753.2:n.1043-964del
NM_002381.4:c.1169-964del (MATN3) NP_002372.1:n.1169-964del
NR_110235.1:n.292-983del (WDR35-DT)
NM_002381.5:c.1169-964del (MATN3) MANE Select NP_002372.1:n.1169-964del