Canonical Allele Identifier: CA2615724645

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790132_102790133insA , CM000673.2:g.102790132_102790133insA GRCh38
NC_000011.9:g.102660863_102660864insA , CM000673.1:g.102660863_102660864insA GRCh37
NC_000011.8:g.102166073_102166074insA NCBI36
NG_011740.1:g.13103_13104insT
NG_011740.2:g.13103_13104insT

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*279_*280insT (MMP1) MANE Select ENSP00000322788.6:n.*279_*280insT
ENST00000680179.1:n.867_868insT (MMP1)
ENST00000681445.1:n.863_864insT (MMP1)
ENST00000681643.1:n.889_890insT (MMP1)
ENST00000315274.6:c.*279_*280insT (MMP1) ENSP00000322788.6:n.*279_*280insT
ENST00000371455.7:n.325-7892_325-7891insA (WTAPP1)
ENST00000525739.6:n.390-3013_390-3012insA (WTAPP1)
ENST00000544704.1:n.344+6068_344+6069insA (WTAPP1)
NM_001145938.1:c.*279_*280insT (MMP1) NP_001139410.1:n.*279_*280insT
NM_002421.3:c.*279_*280insT (MMP1) NP_002412.1:n.*279_*280insT
NR_038390.1:n.390-3013_390-3012insA (WTAPP1)
NM_002421.4:c.*279_*280insT (MMP1) MANE Select NP_002412.1:n.*279_*280insT
NM_001145938.2:c.*279_*280insT (MMP1) NP_001139410.1:n.*279_*280insT