Canonical Allele Identifier: CA2493007792
Gene: MATN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005703T= , CM000664.2:g.20005703T= GRCh38
NC_000002.11:g.20205464T= , CM000664.1:g.20205464T= GRCh37
NC_000002.10:g.20068945T= NCBI36
NG_008087.1:g.11992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.790+41A= MANE Select ENSP00000383894.3:n.790+41A=
ENST00000407540.7:c.790+41A= ENSP00000383894.3:n.790+41A=
ENST00000421259.2:c.790+41A= ENSP00000398753.2:n.790+41A=
NM_002381.4:c.790+41A= NP_002372.1:n.790+41A=
NM_002381.5:c.790+41A= MANE Select NP_002372.1:n.790+41A=