Canonical Allele Identifier: CA345950362
Gene: MATN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005749A>T , CM000664.2:g.20005749A>T GRCh38
NC_000002.11:g.20205510A>T , CM000664.1:g.20205510A>T GRCh37
NC_000002.10:g.20068991A>T NCBI36
NG_008087.1:g.11946T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.785T>A MANE Select ENSP00000383894.3:p.Phe262Tyr
ENST00000407540.7:c.785T>A ENSP00000383894.3:p.Phe262Tyr
ENST00000421259.2:c.785T>A ENSP00000398753.2:p.Phe262Tyr
NM_002381.4:c.785T>A NP_002372.1:p.Phe262Tyr
NM_002381.5:c.785T>A MANE Select NP_002372.1:p.Phe262Tyr