Canonical Allele Identifier: CA2615724879

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790234G>T , CM000673.2:g.102790234G>T GRCh38
NC_000011.9:g.102660965G>T , CM000673.1:g.102660965G>T GRCh37
NC_000011.8:g.102166175G>T NCBI36
NG_011740.1:g.13002C>A
NG_011740.2:g.13002C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*178C>A (MMP1) MANE Select ENSP00000322788.6:n.*178C>A
ENST00000680179.1:n.766C>A (MMP1)
ENST00000681445.1:n.762C>A (MMP1)
ENST00000681643.1:n.788C>A (MMP1)
ENST00000315274.6:c.*178C>A (MMP1) ENSP00000322788.6:n.*178C>A
ENST00000371455.7:n.325-7790G>T (WTAPP1)
ENST00000525739.6:n.390-2911G>T (WTAPP1)
ENST00000544704.1:n.344+6170G>T (WTAPP1)
NM_001145938.1:c.*178C>A (MMP1) NP_001139410.1:n.*178C>A
NM_002421.3:c.*178C>A (MMP1) NP_002412.1:n.*178C>A
NR_038390.1:n.390-2911G>T (WTAPP1)
NM_002421.4:c.*178C>A (MMP1) MANE Select NP_002412.1:n.*178C>A
NM_001145938.2:c.*178C>A (MMP1) NP_001139410.1:n.*178C>A