Canonical Allele Identifier: CA2223714687
Gene: MMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55491907G= , CM000678.2:g.55491907G= GRCh38
NC_000016.9:g.55525819G= , CM000678.1:g.55525819G= GRCh37
NC_000016.8:g.54083320G= NCBI36
NG_008989.1:g.17739G=

Transcript Alleles

HGVS Amino-acid Change
NM_004530.6:c.1287G= MANE Select NP_004521.1:p.Lys429=
ENST00000219070.9:c.1287G= MANE Select ENSP00000219070.4:p.Lys429=
NM_001127891.2:c.1137G= NP_001121363.1:p.Lys379=
NM_001127891.3:c.1137G= NP_001121363.1:p.Lys379=
NM_001302508.1:c.1059G= NP_001289437.1:p.Lys353=
NM_001302509.1:c.1059G= NP_001289438.1:p.Lys353=
NM_001302509.2:c.1059G= NP_001289438.1:p.Lys353=
NM_001302510.1:c.1059G= NP_001289439.1:p.Lys353=
NM_001302510.2:c.1059G= NP_001289439.1:p.Lys353=
NM_004530.5:c.1287G= NP_004521.1:p.Lys429=
ENST00000219070.8:c.1287G= ENSP00000219070.4:p.Lys429=
ENST00000437642.6:c.1137G= ENSP00000394237.2:p.Lys379=
ENST00000543485.5:c.1059G= ENSP00000444143.1:p.Lys353=
ENST00000570283.1:c.162G= ENSP00000456518.1:p.Lys54=
ENST00000570308.5:c.1059G= ENSP00000461421.1:p.Lys353=