Canonical Allele Identifier: CA8060357

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55491847G>A , CM000678.2:g.55491847G>A	GRCh38
NC_000016.9:g.55525759G>A , CM000678.1:g.55525759G>A	GRCh37
NC_000016.8:g.54083260G>A	NCBI36
NG_008989.1:g.17679G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.1227G>A MANE Select	NP_004521.1:p.Met409Ile
ENST00000219070.9:c.1227G>A MANE Select	ENSP00000219070.4:p.Met409Ile
NM_001127891.2:c.1077G>A	NP_001121363.1:p.Met359Ile
NM_001127891.3:c.1077G>A	NP_001121363.1:p.Met359Ile
NM_001302508.1:c.999G>A	NP_001289437.1:p.Met333Ile
NM_001302509.1:c.999G>A	NP_001289438.1:p.Met333Ile
NM_001302509.2:c.999G>A	NP_001289438.1:p.Met333Ile
NM_001302510.1:c.999G>A	NP_001289439.1:p.Met333Ile
NM_001302510.2:c.999G>A	NP_001289439.1:p.Met333Ile
NM_004530.5:c.1227G>A	NP_004521.1:p.Met409Ile
ENST00000219070.8:c.1227G>A	ENSP00000219070.4:p.Met409Ile
ENST00000437642.6:c.1077G>A	ENSP00000394237.2:p.Met359Ile
ENST00000543485.5:c.999G>A	ENSP00000444143.1:p.Met333Ile
ENST00000570283.1:c.102G>A	ENSP00000456518.1:p.Met34Ile
ENST00000570308.5:c.999G>A	ENSP00000461421.1:p.Met333Ile