Canonical Allele Identifier: CA2749074286
Gene: MATN3 HGNC NCBI
WDR35-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19998339_19998340insCAGCAGCGGCTTGCCGGCAAAGCGCTGGCACAGG , CM000664.2:g.19998339_19998340insCAGCAGCGGCTTGCCGGCAAAGCGCTGGCACAGG GRCh38
NC_000002.11:g.20198100_20198101insCAGCAGCGGCTTGCCGGCAAAGCGCTGGCACAGG , CM000664.1:g.20198100_20198101insCAGCAGCGGCTTGCCGGCAAAGCGCTGGCACAGG GRCh37
NC_000002.10:g.20061581_20061582insCAGCAGCGGCTTGCCGGCAAAGCGCTGGCACAGG NCBI36
NG_008087.1:g.19355_19356insCCTGTGCCAGCGCTTTGCCGGCAAGCCGCTGCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCCGGCAAGCCGCTGCTG (MATN3) MANE Select ENSP00000383894.3:n.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCC...
ENST00000407540.7:c.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCCGGCAAGCCGCTGCTG (MATN3) ENSP00000383894.3:n.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCC...
ENST00000421259.2:c.1043-1081_1043-1080insCCTGTGCCAGCGCTTTGCCGGCAAGCCGCTGCTG (MATN3) ENSP00000398753.2:n.1043-1081_1043-1080insCCTGTGCCAGCGCTTTGCC...
NM_002381.4:c.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCCGGCAAGCCGCTGCTG (MATN3) NP_002372.1:n.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCCGGCAAG...
NR_110235.1:n.292-867_292-866insCAGCAGCGGCTTGCCGGCAAAGCGCTGGCACAGG (WDR35-DT)
NM_002381.5:c.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCCGGCAAGCCGCTGCTG (MATN3) MANE Select NP_002372.1:n.1169-1081_1169-1080insCCTGTGCCAGCGCTTTGCCGGCAAG...