Canonical Allele Identifier: CA2223715392

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55493201G= , CM000678.2:g.55493201G=	GRCh38
NC_000016.9:g.55527113G= , CM000678.1:g.55527113G=	GRCh37
NC_000016.8:g.54084614G=	NCBI36
NG_008989.1:g.19033G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.1380G= MANE Select	NP_004521.1:p.Thr460=
ENST00000219070.9:c.1380G= MANE Select	ENSP00000219070.4:p.Thr460=
NM_001127891.2:c.1230G=	NP_001121363.1:p.Thr410=
NM_001127891.3:c.1230G=	NP_001121363.1:p.Thr410=
NM_001302508.1:c.1152G=	NP_001289437.1:p.Thr384=
NM_001302509.1:c.1152G=	NP_001289438.1:p.Thr384=
NM_001302509.2:c.1152G=	NP_001289438.1:p.Thr384=
NM_001302510.1:c.1152G=	NP_001289439.1:p.Thr384=
NM_001302510.2:c.1152G=	NP_001289439.1:p.Thr384=
NM_004530.5:c.1380G=	NP_004521.1:p.Thr460=
ENST00000219070.8:c.1380G=	ENSP00000219070.4:p.Thr460=
ENST00000437642.6:c.1230G=	ENSP00000394237.2:p.Thr410=
ENST00000543485.5:c.1152G=	ENSP00000444143.1:p.Thr384=
ENST00000570283.1:c.255G=	ENSP00000456518.1:p.Thr85=
ENST00000570308.5:c.1152G=	ENSP00000461421.1:p.Thr384=