Canonical Allele Identifier: CA2493007956
Gene: MATN3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20006050A= , CM000664.2:g.20006050A= GRCh38
NC_000002.11:g.20205811A= , CM000664.1:g.20205811A= GRCh37
NC_000002.10:g.20069292A= NCBI36
NG_008087.1:g.11645T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.484T= MANE Select ENSP00000383894.3:p.Ser162=
ENST00000407540.7:c.484T= ENSP00000383894.3:p.Ser162=
ENST00000421259.2:c.484T= ENSP00000398753.2:p.Ser162=
NM_002381.4:c.484T= NP_002372.1:p.Ser162=
NM_002381.5:c.484T= MANE Select NP_002372.1:p.Ser162=
Search 100 bp 5'
Search 100 bp 3'