Canonical Allele Identifier: CA227360015

Linked Data

dbSNP Id: rs770224773
MyVariant Identifiers: chr11:g.102790070C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790070C>T , CM000673.2:g.102790070C>T GRCh38
NC_000011.9:g.102660801C>T , CM000673.1:g.102660801C>T GRCh37
NC_000011.8:g.102166011C>T NCBI36
NG_011740.1:g.13166G>A
NG_011740.2:g.13166G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*342G>A (MMP1) MANE Select ENSP00000322788.6:n.*342G>A
ENST00000680179.1:n.930G>A (MMP1)
ENST00000681445.1:n.926G>A (MMP1)
ENST00000681643.1:n.952G>A (MMP1)
ENST00000315274.6:c.*342G>A (MMP1) ENSP00000322788.6:n.*342G>A
ENST00000371455.7:n.325-7954C>T (WTAPP1)
ENST00000525739.6:n.390-3075C>T (WTAPP1)
ENST00000544704.1:n.344+6006C>T (WTAPP1)
NM_001145938.1:c.*342G>A (MMP1) NP_001139410.1:n.*342G>A
NM_002421.3:c.*342G>A (MMP1) NP_002412.1:n.*342G>A
NR_038390.1:n.390-3075C>T (WTAPP1)
NM_002421.4:c.*342G>A (MMP1) MANE Select NP_002412.1:n.*342G>A
NM_001145938.2:c.*342G>A (MMP1) NP_001139410.1:n.*342G>A