Canonical Allele Identifier: CA2493007889

Gene: MATN3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.20005908C= , CM000664.2:g.20005908C=	GRCh38
NC_000002.11:g.20205669C= , CM000664.1:g.20205669C=	GRCh37
NC_000002.10:g.20069150C=	NCBI36
NG_008087.1:g.11787G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407540.8:c.626G= MANE Select	ENSP00000383894.3:p.Arg209=
ENST00000407540.7:c.626G=	ENSP00000383894.3:p.Arg209=
ENST00000421259.2:c.626G=	ENSP00000398753.2:p.Arg209=
NM_002381.4:c.626G=	NP_002372.1:p.Arg209=
NM_002381.5:c.626G= MANE Select	NP_002372.1:p.Arg209=