Canonical Allele Identifier: CA941623944

Linked Data

dbSNP Id: rs1858012762

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790973del , CM000673.2:g.102790973del GRCh38
NC_000011.9:g.102661704del , CM000673.1:g.102661704del GRCh37
NC_000011.8:g.102166914del NCBI36
NG_011740.1:g.12266del
NG_011740.2:g.12266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.1197-164del (MMP1) MANE Select ENSP00000322788.6:n.1197-164del
ENST00000680179.1:n.375-164del (MMP1)
ENST00000681445.1:n.371-164del (MMP1)
ENST00000681643.1:n.397-164del (MMP1)
ENST00000315274.6:c.1197-164del (MMP1) ENSP00000322788.6:n.1197-164del
ENST00000371455.7:n.325-7051del (WTAPP1)
ENST00000525739.6:n.390-2172del (WTAPP1)
ENST00000544704.1:n.344+6909del (WTAPP1)
NM_001145938.1:c.999-164del (MMP1) NP_001139410.1:n.999-164del
NM_002421.3:c.1197-164del (MMP1) NP_002412.1:n.1197-164del
NR_038390.1:n.390-2172del (WTAPP1)
NM_002421.4:c.1197-164del (MMP1) MANE Select NP_002412.1:n.1197-164del
NM_001145938.2:c.999-164del (MMP1) NP_001139410.1:n.999-164del