Canonical Allele Identifier: CA2223717725

Gene: MMP2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55498546T>G , CM000678.2:g.55498546T>G	GRCh38
NC_000016.9:g.55532458T>G , CM000678.1:g.55532458T>G	GRCh37
NC_000016.8:g.54089959T>G	NCBI36
NG_008989.1:g.24378T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.1769+98T>G MANE Select	ENSP00000219070.4:n.1769+98T>G
ENST00000219070.8:c.1769+98T>G	ENSP00000219070.4:n.1769+98T>G
ENST00000437642.6:c.1619+98T>G	ENSP00000394237.2:n.1619+98T>G
ENST00000543485.5:c.1541+98T>G	ENSP00000444143.1:n.1541+98T>G
ENST00000570283.1:c.644+98T>G	ENSP00000456518.1:n.644+98T>G
ENST00000570308.5:c.1541+98T>G	ENSP00000461421.1:n.1541+98T>G
NM_001127891.2:c.1619+98T>G	NP_001121363.1:n.1619+98T>G
NM_001302508.1:c.1541+98T>G	NP_001289437.1:n.1541+98T>G
NM_001302509.1:c.1541+98T>G	NP_001289438.1:n.1541+98T>G
NM_001302510.1:c.1541+98T>G	NP_001289439.1:n.1541+98T>G
NM_004530.5:c.1769+98T>G	NP_004521.1:n.1769+98T>G
NM_004530.6:c.1769+98T>G MANE Select	NP_004521.1:n.1769+98T>G
NM_001127891.3:c.1619+98T>G	NP_001121363.1:n.1619+98T>G
NM_001302509.2:c.1541+98T>G	NP_001289438.1:n.1541+98T>G
NM_001302510.2:c.1541+98T>G	NP_001289439.1:n.1541+98T>G