Canonical Allele Identifier: CA2223719105

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55505702A= , CM000678.2:g.55505702A=	GRCh38
NC_000016.9:g.55539614A= , CM000678.1:g.55539614A=	GRCh37
NC_000016.8:g.54097115A=	NCBI36
NG_008989.1:g.31534A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.*260A= MANE Select	NP_004521.1:n.*260A=
ENST00000219070.9:c.*260A= MANE Select	ENSP00000219070.4:n.*260A=
NM_001127891.2:c.*260A=	NP_001121363.1:n.*260A=
NM_001127891.3:c.*260A=	NP_001121363.1:n.*260A=
NM_001302508.1:c.*260A=	NP_001289437.1:n.*260A=
NM_001302509.1:c.*260A=	NP_001289438.1:n.*260A=
NM_001302509.2:c.*260A=	NP_001289438.1:n.*260A=
NM_001302510.1:c.*260A=	NP_001289439.1:n.*260A=
NM_001302510.2:c.*260A=	NP_001289439.1:n.*260A=
NM_004530.5:c.*260A=	NP_004521.1:n.*260A=
ENST00000219070.8:c.*260A=	ENSP00000219070.4:n.*260A=
ENST00000437642.6:c.*260A=	ENSP00000394237.2:n.*260A=
ENST00000566564.1:c.205+123A=
ENST00000570308.5:c.*260A=	ENSP00000461421.1:n.*260A=