Canonical Allele Identifier: CA2793420717

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790214_102790215insTTTTTTTT , CM000673.2:g.102790214_102790215insTTTTTTTT GRCh38
NC_000011.9:g.102660945_102660946insTTTTTTTT , CM000673.1:g.102660945_102660946insTTTTTTTT GRCh37
NC_000011.8:g.102166155_102166156insTTTTTTTT NCBI36
NG_011740.1:g.13024_13025insAAAAAAAA
NG_011740.2:g.13024_13025insAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.*200_*201insAAAAAAAA (MMP1) MANE Select ENSP00000322788.6:n.*200_*201insAAAAAAAA
ENST00000680179.1:n.788_789insAAAAAAAA (MMP1)
ENST00000681445.1:n.784_785insAAAAAAAA (MMP1)
ENST00000681643.1:n.810_811insAAAAAAAA (MMP1)
ENST00000315274.6:c.*200_*201insAAAAAAAA (MMP1) ENSP00000322788.6:n.*200_*201insAAAAAAAA
ENST00000371455.7:n.325-7810_325-7809insTTTTTTTT (WTAPP1)
ENST00000525739.6:n.390-2931_390-2930insTTTTTTTT (WTAPP1)
ENST00000544704.1:n.344+6150_344+6151insTTTTTTTT (WTAPP1)
NM_001145938.1:c.*200_*201insAAAAAAAA (MMP1) NP_001139410.1:n.*200_*201insAAAAAAAA
NM_002421.3:c.*200_*201insAAAAAAAA (MMP1) NP_002412.1:n.*200_*201insAAAAAAAA
NR_038390.1:n.390-2931_390-2930insTTTTTTTT (WTAPP1)
NM_002421.4:c.*200_*201insAAAAAAAA (MMP1) MANE Select NP_002412.1:n.*200_*201insAAAAAAAA
NM_001145938.2:c.*200_*201insAAAAAAAA (MMP1) NP_001139410.1:n.*200_*201insAAAAAAAA