Canonical Allele Identifier: CA395936726

Gene: MMP2

Linked Data

• MyVariant Identifiers: chr16:g.55525822C>A (hg19) ; chr16:g.55491910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55491910C>A , CM000678.2:g.55491910C>A	GRCh38
NC_000016.9:g.55525822C>A , CM000678.1:g.55525822C>A	GRCh37
NC_000016.8:g.54083323C>A	NCBI36
NG_008989.1:g.17742C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000219070.9:c.1290C>A MANE Select	ENSP00000219070.4:p.Asn430Lys
ENST00000219070.8:c.1290C>A	ENSP00000219070.4:p.Asn430Lys
ENST00000437642.6:c.1140C>A	ENSP00000394237.2:p.Asn380Lys
ENST00000543485.5:c.1062C>A	ENSP00000444143.1:p.Asn354Lys
ENST00000570283.1:c.165C>A	ENSP00000456518.1:p.Asn55Lys
ENST00000570308.5:c.1062C>A	ENSP00000461421.1:p.Asn354Lys
NM_001127891.2:c.1140C>A	NP_001121363.1:p.Asn380Lys
NM_001302508.1:c.1062C>A	NP_001289437.1:p.Asn354Lys
NM_001302509.1:c.1062C>A	NP_001289438.1:p.Asn354Lys
NM_001302510.1:c.1062C>A	NP_001289439.1:p.Asn354Lys
NM_004530.5:c.1290C>A	NP_004521.1:p.Asn430Lys
NM_004530.6:c.1290C>A MANE Select	NP_004521.1:p.Asn430Lys
NM_001127891.3:c.1140C>A	NP_001121363.1:p.Asn380Lys
NM_001302509.2:c.1062C>A	NP_001289438.1:p.Asn354Lys
NM_001302510.2:c.1062C>A	NP_001289439.1:p.Asn354Lys