Canonical Allele Identifier: CA763243777
Gene: MATN3 HGNC NCBI

Linked Data

dbSNP Id: rs1160416035
gnomAD v3: 2-20005582-GCA-G
gnomAD v4: 2-20005582-GCA-G
MyVariant Identifiers: chr2:g.20205344_20205345del (hg19) chr2:g.20005583_20005584del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005588_20005589del , CM000664.2:g.20005588_20005589del GRCh38
NC_000002.11:g.20205349_20205350del , CM000664.1:g.20205349_20205350del GRCh37
NC_000002.10:g.20068830_20068831del NCBI36
NG_008087.1:g.12111_12112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.790+160_790+161del MANE Select ENSP00000383894.3:n.790+160_790+161del
ENST00000407540.7:c.790+160_790+161del ENSP00000383894.3:n.790+160_790+161del
ENST00000421259.2:c.790+160_790+161del ENSP00000398753.2:n.790+160_790+161del
NM_002381.4:c.790+160_790+161del NP_002372.1:n.790+160_790+161del
NM_002381.5:c.790+160_790+161del MANE Select NP_002372.1:n.790+160_790+161del
Search 100 bp 5'
Search 100 bp 3'