Canonical Allele Identifier: CA2615724823

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790208A>G , CM000673.2:g.102790208A>G GRCh38
NC_000011.9:g.102660939A>G , CM000673.1:g.102660939A>G GRCh37
NC_000011.8:g.102166149A>G NCBI36
NG_011740.1:g.13028T>C
NG_011740.2:g.13028T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.*204T>C (MMP1) MANE Select ENSP00000322788.6:n.*204T>C
ENST00000680179.1:n.792T>C (MMP1)
ENST00000681445.1:n.788T>C (MMP1)
ENST00000681643.1:n.814T>C (MMP1)
ENST00000315274.6:c.*204T>C (MMP1) ENSP00000322788.6:n.*204T>C
ENST00000371455.7:n.325-7816A>G (WTAPP1)
ENST00000525739.6:n.390-2937A>G (WTAPP1)
ENST00000544704.1:n.344+6144A>G (WTAPP1)
NM_001145938.1:c.*204T>C (MMP1) NP_001139410.1:n.*204T>C
NM_002421.3:c.*204T>C (MMP1) NP_002412.1:n.*204T>C
NR_038390.1:n.390-2937A>G (WTAPP1)
NM_002421.4:c.*204T>C (MMP1) MANE Select NP_002412.1:n.*204T>C
NM_001145938.2:c.*204T>C (MMP1) NP_001139410.1:n.*204T>C