Canonical Allele Identifier: CA345950389
Gene: MATN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005760G>T , CM000664.2:g.20005760G>T GRCh38
NC_000002.11:g.20205521G>T , CM000664.1:g.20205521G>T GRCh37
NC_000002.10:g.20069002G>T NCBI36
NG_008087.1:g.11935C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.774C>A MANE Select ENSP00000383894.3:p.Phe258Leu
ENST00000407540.7:c.774C>A ENSP00000383894.3:p.Phe258Leu
ENST00000421259.2:c.774C>A ENSP00000398753.2:p.Phe258Leu
NM_002381.4:c.774C>A NP_002372.1:p.Phe258Leu
NM_002381.5:c.774C>A MANE Select NP_002372.1:p.Phe258Leu