Canonical Allele Identifier: CA2223711660

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55485695C= , CM000678.2:g.55485695C=	GRCh38
NC_000016.9:g.55519607C= , CM000678.1:g.55519607C=	GRCh37
NC_000016.8:g.54077108C=	NCBI36
NG_008989.1:g.11527C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.750C= MANE Select	NP_004521.1:p.Thr250=
ENST00000219070.9:c.750C= MANE Select	ENSP00000219070.4:p.Thr250=
NM_001127891.2:c.600C=	NP_001121363.1:p.Thr200=
NM_001127891.3:c.600C=	NP_001121363.1:p.Thr200=
NM_001302508.1:c.522C=	NP_001289437.1:p.Thr174=
NM_001302509.1:c.522C=	NP_001289438.1:p.Thr174=
NM_001302509.2:c.522C=	NP_001289438.1:p.Thr174=
NM_001302510.1:c.522C=	NP_001289439.1:p.Thr174=
NM_001302510.2:c.522C=	NP_001289439.1:p.Thr174=
NM_004530.5:c.750C=	NP_004521.1:p.Thr250=
ENST00000219070.8:c.750C=	ENSP00000219070.4:p.Thr250=
ENST00000437642.6:c.600C=	ENSP00000394237.2:p.Thr200=
ENST00000543485.5:c.522C=	ENSP00000444143.1:p.Thr174=
ENST00000564864.5:c.522C=	ENSP00000456096.1:p.Thr174=
ENST00000570308.5:c.522C=	ENSP00000461421.1:p.Thr174=