Canonical Allele Identifier: CA8060591

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55502811G>T , CM000678.2:g.55502811G>T	GRCh38
NC_000016.9:g.55536723G>T , CM000678.1:g.55536723G>T	GRCh37
NC_000016.8:g.54094224G>T	NCBI36
NG_008989.1:g.28643G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.1802G>T MANE Select	ENSP00000219070.4:p.Gly601Val
ENST00000219070.8:c.1802G>T	ENSP00000219070.4:p.Gly601Val
ENST00000437642.6:c.1652G>T	ENSP00000394237.2:p.Gly551Val
ENST00000543485.5:c.1574G>T	ENSP00000444143.1:p.Gly525Val
ENST00000570283.1:c.677G>T	ENSP00000456518.1:p.Gly226Val
ENST00000570308.5:c.1574G>T	ENSP00000461421.1:p.Gly525Val
NM_001127891.2:c.1652G>T	NP_001121363.1:p.Gly551Val
NM_001302508.1:c.1574G>T	NP_001289437.1:p.Gly525Val
NM_001302509.1:c.1574G>T	NP_001289438.1:p.Gly525Val
NM_001302510.1:c.1574G>T	NP_001289439.1:p.Gly525Val
NM_004530.5:c.1802G>T	NP_004521.1:p.Gly601Val
NM_004530.6:c.1802G>T MANE Select	NP_004521.1:p.Gly601Val
NM_001127891.3:c.1652G>T	NP_001121363.1:p.Gly551Val
NM_001302509.2:c.1574G>T	NP_001289438.1:p.Gly525Val
NM_001302510.2:c.1574G>T	NP_001289439.1:p.Gly525Val