Canonical Allele Identifier: CA395936725

Gene: MMP2

Linked Data

• MyVariant Identifiers: chr16:g.55525821A>T (hg19) ; chr16:g.55491909A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55491909A>T , CM000678.2:g.55491909A>T	GRCh38
NC_000016.9:g.55525821A>T , CM000678.1:g.55525821A>T	GRCh37
NC_000016.8:g.54083322A>T	NCBI36
NG_008989.1:g.17741A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.1289A>T MANE Select	ENSP00000219070.4:p.Asn430Ile
ENST00000219070.8:c.1289A>T	ENSP00000219070.4:p.Asn430Ile
ENST00000437642.6:c.1139A>T	ENSP00000394237.2:p.Asn380Ile
ENST00000543485.5:c.1061A>T	ENSP00000444143.1:p.Asn354Ile
ENST00000570283.1:c.164A>T	ENSP00000456518.1:p.Asn55Ile
ENST00000570308.5:c.1061A>T	ENSP00000461421.1:p.Asn354Ile
NM_001127891.2:c.1139A>T	NP_001121363.1:p.Asn380Ile
NM_001302508.1:c.1061A>T	NP_001289437.1:p.Asn354Ile
NM_001302509.1:c.1061A>T	NP_001289438.1:p.Asn354Ile
NM_001302510.1:c.1061A>T	NP_001289439.1:p.Asn354Ile
NM_004530.5:c.1289A>T	NP_004521.1:p.Asn430Ile
NM_004530.6:c.1289A>T MANE Select	NP_004521.1:p.Asn430Ile
NM_001127891.3:c.1139A>T	NP_001121363.1:p.Asn380Ile
NM_001302509.2:c.1061A>T	NP_001289438.1:p.Asn354Ile
NM_001302510.2:c.1061A>T	NP_001289439.1:p.Asn354Ile