Canonical Allele Identifier: CA2493007736
Gene: MATN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005588_20005590delinsACG , CM000664.2:g.20005588_20005590delinsACG GRCh38
NC_000002.11:g.20205349_20205351delinsACG , CM000664.1:g.20205349_20205351delinsACG GRCh37
NC_000002.10:g.20068830_20068832delinsACG NCBI36
NG_008087.1:g.12105_12107delinsCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.790+154_790+156delinsCGT MANE Select ENSP00000383894.3:n.790+154_790+156delinsCGT
ENST00000407540.7:c.790+154_790+156delinsCGT ENSP00000383894.3:n.790+154_790+156delinsCGT
ENST00000421259.2:c.790+154_790+156delinsCGT ENSP00000398753.2:n.790+154_790+156delinsCGT
NM_002381.4:c.790+154_790+156delinsCGT NP_002372.1:n.790+154_790+156delinsCGT
NM_002381.5:c.790+154_790+156delinsCGT MANE Select NP_002372.1:n.790+154_790+156delinsCGT