Canonical Allele Identifier: CA2493007798
Gene: MATN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005717_20005718delinsGT , CM000664.2:g.20005717_20005718delinsGT GRCh38
NC_000002.11:g.20205478_20205479delinsGT , CM000664.1:g.20205478_20205479delinsGT GRCh37
NC_000002.10:g.20068959_20068960delinsGT NCBI36
NG_008087.1:g.11977_11978delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.790+26_790+27delinsAC MANE Select ENSP00000383894.3:n.790+26_790+27delinsAC
ENST00000407540.7:c.790+26_790+27delinsAC ENSP00000383894.3:n.790+26_790+27delinsAC
ENST00000421259.2:c.790+26_790+27delinsAC ENSP00000398753.2:n.790+26_790+27delinsAC
NM_002381.4:c.790+26_790+27delinsAC NP_002372.1:n.790+26_790+27delinsAC
NM_002381.5:c.790+26_790+27delinsAC MANE Select NP_002372.1:n.790+26_790+27delinsAC