Canonical Allele Identifier: CA2615724512

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790048G>T , CM000673.2:g.102790048G>T GRCh38
NC_000011.9:g.102660779G>T , CM000673.1:g.102660779G>T GRCh37
NC_000011.8:g.102165989G>T NCBI36
NG_011740.1:g.13188C>A
NG_011740.2:g.13188C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*364C>A (MMP1) MANE Select ENSP00000322788.6:n.*364C>A
ENST00000680179.1:n.952C>A (MMP1)
ENST00000681445.1:n.948C>A (MMP1)
ENST00000681643.1:n.974C>A (MMP1)
ENST00000315274.6:c.*364C>A (MMP1) ENSP00000322788.6:n.*364C>A
ENST00000371455.7:n.325-7976G>T (WTAPP1)
ENST00000525739.6:n.390-3097G>T (WTAPP1)
ENST00000544704.1:n.344+5984G>T (WTAPP1)
NM_001145938.1:c.*364C>A (MMP1) NP_001139410.1:n.*364C>A
NM_002421.3:c.*364C>A (MMP1) NP_002412.1:n.*364C>A
NR_038390.1:n.390-3097G>T (WTAPP1)
NM_002421.4:c.*364C>A (MMP1) MANE Select NP_002412.1:n.*364C>A
NM_001145938.2:c.*364C>A (MMP1) NP_001139410.1:n.*364C>A