Canonical Allele Identifier: CA2724643529
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1858013357
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790989T>A , CM000673.2:g.102790989T>A GRCh38
NC_000011.9:g.102661720T>A , CM000673.1:g.102661720T>A GRCh37
NC_000011.8:g.102166930T>A NCBI36
NG_011740.1:g.12247A>T
NG_011740.2:g.12247A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.1197-183A>T (MMP1) MANE Select ENSP00000322788.6:n.1197-183A>T
ENST00000680179.1:n.375-183A>T (MMP1)
ENST00000681445.1:n.371-183A>T (MMP1)
ENST00000681643.1:n.397-183A>T (MMP1)
ENST00000315274.6:c.1197-183A>T (MMP1) ENSP00000322788.6:n.1197-183A>T
ENST00000371455.7:n.325-7035T>A (WTAPP1)
ENST00000525739.6:n.390-2156T>A (WTAPP1)
ENST00000544704.1:n.344+6925T>A (WTAPP1)
NM_001145938.1:c.999-183A>T (MMP1) NP_001139410.1:n.999-183A>T
NM_002421.3:c.1197-183A>T (MMP1) NP_002412.1:n.1197-183A>T
NR_038390.1:n.390-2156T>A (WTAPP1)
NM_002421.4:c.1197-183A>T (MMP1) MANE Select NP_002412.1:n.1197-183A>T
NM_001145938.2:c.999-183A>T (MMP1) NP_001139410.1:n.999-183A>T
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Search 100 bp 3'