Canonical Allele Identifier: CA2223714656

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55491830G= , CM000678.2:g.55491830G=	GRCh38
NC_000016.9:g.55525742G= , CM000678.1:g.55525742G=	GRCh37
NC_000016.8:g.54083243G=	NCBI36
NG_008989.1:g.17662G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.1210G= MANE Select	NP_004521.1:p.Glu404=
ENST00000219070.9:c.1210G= MANE Select	ENSP00000219070.4:p.Glu404=
NM_001127891.2:c.1060G=	NP_001121363.1:p.Glu354=
NM_001127891.3:c.1060G=	NP_001121363.1:p.Glu354=
NM_001302508.1:c.982G=	NP_001289437.1:p.Glu328=
NM_001302509.1:c.982G=	NP_001289438.1:p.Glu328=
NM_001302509.2:c.982G=	NP_001289438.1:p.Glu328=
NM_001302510.1:c.982G=	NP_001289439.1:p.Glu328=
NM_001302510.2:c.982G=	NP_001289439.1:p.Glu328=
NM_004530.5:c.1210G=	NP_004521.1:p.Glu404=
ENST00000219070.8:c.1210G=	ENSP00000219070.4:p.Glu404=
ENST00000437642.6:c.1060G=	ENSP00000394237.2:p.Glu354=
ENST00000543485.5:c.982G=	ENSP00000444143.1:p.Glu328=
ENST00000570283.1:c.85G=	ENSP00000456518.1:p.Glu29=
ENST00000570308.5:c.982G=	ENSP00000461421.1:p.Glu328=