Canonical Allele Identifier: CA2793420784

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790870_102790871insAGAT , CM000673.2:g.102790870_102790871insAGAT GRCh38
NC_000011.9:g.102661601_102661602insAGAT , CM000673.1:g.102661601_102661602insAGAT GRCh37
NC_000011.8:g.102166811_102166812insAGAT NCBI36
NG_011740.1:g.12365_12366insATCT
NG_011740.2:g.12365_12366insATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.1197-65_1197-64insATCT (MMP1) MANE Select ENSP00000322788.6:n.1197-65_1197-64insATCT
ENST00000680179.1:n.375-65_375-64insATCT (MMP1)
ENST00000681445.1:n.371-65_371-64insATCT (MMP1)
ENST00000681643.1:n.397-65_397-64insATCT (MMP1)
ENST00000315274.6:c.1197-65_1197-64insATCT (MMP1) ENSP00000322788.6:n.1197-65_1197-64insATCT
ENST00000371455.7:n.325-7154_325-7153insAGAT (WTAPP1)
ENST00000525739.6:n.390-2275_390-2274insAGAT (WTAPP1)
ENST00000544704.1:n.344+6806_344+6807insAGAT (WTAPP1)
NM_001145938.1:c.999-65_999-64insATCT (MMP1) NP_001139410.1:n.999-65_999-64insATCT
NM_002421.3:c.1197-65_1197-64insATCT (MMP1) NP_002412.1:n.1197-65_1197-64insATCT
NR_038390.1:n.390-2275_390-2274insAGAT (WTAPP1)
NM_002421.4:c.1197-65_1197-64insATCT (MMP1) MANE Select NP_002412.1:n.1197-65_1197-64insATCT
NM_001145938.2:c.999-65_999-64insATCT (MMP1) NP_001139410.1:n.999-65_999-64insATCT