Canonical Allele Identifier: CA2223710408

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55483026C= , CM000678.2:g.55483026C=	GRCh38
NC_000016.9:g.55516938C= , CM000678.1:g.55516938C=	GRCh37
NC_000016.8:g.54074439C=	NCBI36
NG_008989.1:g.8858C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.271C= MANE Select	ENSP00000219070.4:p.Gln91=
ENST00000219070.8:c.271C=	ENSP00000219070.4:p.Gln91=
ENST00000437642.6:c.121C=	ENSP00000394237.2:p.Gln41=
ENST00000543485.5:c.43C=	ENSP00000444143.1:p.Gln15=
ENST00000564864.5:c.43C=	ENSP00000456096.1:p.Gln15=
ENST00000568715.5:c.43C=	ENSP00000457949.1:p.Gln15=
ENST00000570308.5:c.43C=	ENSP00000461421.1:p.Gln15=
NM_001127891.2:c.121C=	NP_001121363.1:p.Gln41=
NM_001302508.1:c.43C=	NP_001289437.1:p.Gln15=
NM_001302509.1:c.43C=	NP_001289438.1:p.Gln15=
NM_001302510.1:c.43C=	NP_001289439.1:p.Gln15=
NM_004530.5:c.271C=	NP_004521.1:p.Gln91=
NM_004530.6:c.271C= MANE Select	NP_004521.1:p.Gln91=
NM_001127891.3:c.121C=	NP_001121363.1:p.Gln41=
NM_001302509.2:c.43C=	NP_001289438.1:p.Gln15=
NM_001302510.2:c.43C=	NP_001289439.1:p.Gln15=