Canonical Allele Identifier: CA2223719103
Gene: MMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55505702A>T , CM000678.2:g.55505702A>T GRCh38
NC_000016.9:g.55539614A>T , CM000678.1:g.55539614A>T GRCh37
NC_000016.8:g.54097115A>T NCBI36
NG_008989.1:g.31534A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000219070.9:c.*260A>T MANE Select ENSP00000219070.4:n.*260A>T
ENST00000219070.8:c.*260A>T ENSP00000219070.4:n.*260A>T
ENST00000437642.6:c.*260A>T ENSP00000394237.2:n.*260A>T
ENST00000566564.1:c.205+123A>T
ENST00000570308.5:c.*260A>T ENSP00000461421.1:n.*260A>T
NM_001127891.2:c.*260A>T NP_001121363.1:n.*260A>T
NM_001302508.1:c.*260A>T NP_001289437.1:n.*260A>T
NM_001302509.1:c.*260A>T NP_001289438.1:n.*260A>T
NM_001302510.1:c.*260A>T NP_001289439.1:n.*260A>T
NM_004530.5:c.*260A>T NP_004521.1:n.*260A>T
NM_004530.6:c.*260A>T MANE Select NP_004521.1:n.*260A>T
NM_001127891.3:c.*260A>T NP_001121363.1:n.*260A>T
NM_001302509.2:c.*260A>T NP_001289438.1:n.*260A>T
NM_001302510.2:c.*260A>T NP_001289439.1:n.*260A>T