Canonical Allele Identifier: CA2223713376

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55489099T= , CM000678.2:g.55489099T=	GRCh38
NC_000016.9:g.55523011T= , CM000678.1:g.55523011T=	GRCh37
NC_000016.8:g.54080512T=	NCBI36
NG_008989.1:g.14931T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.1006+383T= MANE Select	NP_004521.1:n.1006+383T=
ENST00000219070.9:c.1006+383T= MANE Select	ENSP00000219070.4:n.1006+383T=
NM_001127891.2:c.856+383T=	NP_001121363.1:n.856+383T=
NM_001127891.3:c.856+383T=	NP_001121363.1:n.856+383T=
NM_001302508.1:c.778+383T=	NP_001289437.1:n.778+383T=
NM_001302509.1:c.778+383T=	NP_001289438.1:n.778+383T=
NM_001302509.2:c.778+383T=	NP_001289438.1:n.778+383T=
NM_001302510.1:c.778+383T=	NP_001289439.1:n.778+383T=
NM_001302510.2:c.778+383T=	NP_001289439.1:n.778+383T=
NM_004530.5:c.1006+383T=	NP_004521.1:n.1006+383T=
ENST00000219070.8:c.1006+383T=	ENSP00000219070.4:n.1006+383T=
ENST00000437642.6:c.856+383T=	ENSP00000394237.2:n.856+383T=
ENST00000543485.5:c.778+383T=	ENSP00000444143.1:n.778+383T=
ENST00000570283.1:c.55+383T=	ENSP00000456518.1:n.55+383T=
ENST00000570308.5:c.778+383T=	ENSP00000461421.1:n.778+383T=