Canonical Allele Identifier: CA2497334480

Linked Data

dbSNP Id: rs1857975371

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789960del , CM000673.2:g.102789960del GRCh38
NC_000011.9:g.102660691del , CM000673.1:g.102660691del GRCh37
NC_000011.8:g.102165901del NCBI36
NG_011740.1:g.13279del
NG_011740.2:g.13279del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.*455del (MMP1) MANE Select ENSP00000322788.6:n.*455del
ENST00000680179.1:n.1043del (MMP1)
ENST00000681445.1:n.1039del (MMP1)
ENST00000681643.1:n.1065del (MMP1)
ENST00000315274.6:c.*455del (MMP1) ENSP00000322788.6:n.*455del
ENST00000371455.7:n.325-8064del (WTAPP1)
ENST00000525739.6:n.390-3185del (WTAPP1)
ENST00000544704.1:n.344+5896del (WTAPP1)
NM_001145938.1:c.*455del (MMP1) NP_001139410.1:n.*455del
NM_002421.3:c.*455del (MMP1) NP_002412.1:n.*455del
NR_038390.1:n.390-3185del (WTAPP1)
NM_002421.4:c.*455del (MMP1) MANE Select NP_002412.1:n.*455del
NM_001145938.2:c.*455del (MMP1) NP_001139410.1:n.*455del