Canonical Allele Identifier: CA395931371
Gene: MMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55482934G>C , CM000678.2:g.55482934G>C GRCh38
NC_000016.9:g.55516846G>C , CM000678.1:g.55516846G>C GRCh37
NC_000016.8:g.54074347G>C NCBI36
NG_008989.1:g.8766G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000219070.9:c.179G>C MANE Select ENSP00000219070.4:p.Cys60Ser
ENST00000219070.8:c.179G>C ENSP00000219070.4:p.Cys60Ser
ENST00000437642.6:c.29G>C ENSP00000394237.2:p.Cys10Ser
ENST00000543485.5:c.-50G>C ENSP00000444143.1:n.-50G>C
ENST00000564864.5:c.-50G>C ENSP00000456096.1:n.-50G>C
ENST00000568715.5:c.-50G>C ENSP00000457949.1:n.-50G>C
ENST00000570308.5:c.-50G>C ENSP00000461421.1:n.-50G>C
NM_001127891.2:c.29G>C NP_001121363.1:p.Cys10Ser
NM_001302508.1:c.-50G>C NP_001289437.1:n.-50G>C
NM_001302509.1:c.-50G>C NP_001289438.1:n.-50G>C
NM_001302510.1:c.-50G>C NP_001289439.1:n.-50G>C
NM_004530.5:c.179G>C NP_004521.1:p.Cys60Ser
NM_004530.6:c.179G>C MANE Select NP_004521.1:p.Cys60Ser
NM_001127891.3:c.29G>C NP_001121363.1:p.Cys10Ser
NM_001302509.2:c.-50G>C NP_001289438.1:n.-50G>C
NM_001302510.2:c.-50G>C NP_001289439.1:n.-50G>C