Canonical Allele Identifier: CA2497334621
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1858009956
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790884_102790885del , CM000673.2:g.102790884_102790885del GRCh38
NC_000011.9:g.102661615_102661616del , CM000673.1:g.102661615_102661616del GRCh37
NC_000011.8:g.102166825_102166826del NCBI36
NG_011740.1:g.12351_12352del
NG_011740.2:g.12351_12352del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.1197-79_1197-78del (MMP1) MANE Select ENSP00000322788.6:n.1197-79_1197-78del
ENST00000680179.1:n.375-79_375-78del (MMP1)
ENST00000681445.1:n.371-79_371-78del (MMP1)
ENST00000681643.1:n.397-79_397-78del (MMP1)
ENST00000315274.6:c.1197-79_1197-78del (MMP1) ENSP00000322788.6:n.1197-79_1197-78del
ENST00000371455.7:n.325-7140_325-7139del (WTAPP1)
ENST00000525739.6:n.390-2261_390-2260del (WTAPP1)
ENST00000544704.1:n.344+6820_344+6821del (WTAPP1)
NM_001145938.1:c.999-79_999-78del (MMP1) NP_001139410.1:n.999-79_999-78del
NM_002421.3:c.1197-79_1197-78del (MMP1) NP_002412.1:n.1197-79_1197-78del
NR_038390.1:n.390-2261_390-2260del (WTAPP1)
NM_002421.4:c.1197-79_1197-78del (MMP1) MANE Select NP_002412.1:n.1197-79_1197-78del
NM_001145938.2:c.999-79_999-78del (MMP1) NP_001139410.1:n.999-79_999-78del
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