Canonical Allele Identifier: CA2223710413

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55483035A= , CM000678.2:g.55483035A=	GRCh38
NC_000016.9:g.55516947A= , CM000678.1:g.55516947A=	GRCh37
NC_000016.8:g.54074448A=	NCBI36
NG_008989.1:g.8867A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.280A= MANE Select	ENSP00000219070.4:p.Ile94=
ENST00000219070.8:c.280A=	ENSP00000219070.4:p.Ile94=
ENST00000437642.6:c.130A=	ENSP00000394237.2:p.Ile44=
ENST00000543485.5:c.52A=	ENSP00000444143.1:p.Ile18=
ENST00000564864.5:c.52A=	ENSP00000456096.1:p.Ile18=
ENST00000568715.5:c.52A=	ENSP00000457949.1:p.Ile18=
ENST00000570308.5:c.52A=	ENSP00000461421.1:p.Ile18=
NM_001127891.2:c.130A=	NP_001121363.1:p.Ile44=
NM_001302508.1:c.52A=	NP_001289437.1:p.Ile18=
NM_001302509.1:c.52A=	NP_001289438.1:p.Ile18=
NM_001302510.1:c.52A=	NP_001289439.1:p.Ile18=
NM_004530.5:c.280A=	NP_004521.1:p.Ile94=
NM_004530.6:c.280A= MANE Select	NP_004521.1:p.Ile94=
NM_001127891.3:c.130A=	NP_001121363.1:p.Ile44=
NM_001302509.2:c.52A=	NP_001289438.1:p.Ile18=
NM_001302510.2:c.52A=	NP_001289439.1:p.Ile18=