Canonical Allele Identifier: CA2223711653

Gene: MMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55485677C= , CM000678.2:g.55485677C=	GRCh38
NC_000016.9:g.55519589C= , CM000678.1:g.55519589C=	GRCh37
NC_000016.8:g.54077090C=	NCBI36
NG_008989.1:g.11509C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004530.6:c.732C= MANE Select	NP_004521.1:p.Tyr244=
ENST00000219070.9:c.732C= MANE Select	ENSP00000219070.4:p.Tyr244=
NM_001127891.2:c.582C=	NP_001121363.1:p.Tyr194=
NM_001127891.3:c.582C=	NP_001121363.1:p.Tyr194=
NM_001302508.1:c.504C=	NP_001289437.1:p.Tyr168=
NM_001302509.1:c.504C=	NP_001289438.1:p.Tyr168=
NM_001302509.2:c.504C=	NP_001289438.1:p.Tyr168=
NM_001302510.1:c.504C=	NP_001289439.1:p.Tyr168=
NM_001302510.2:c.504C=	NP_001289439.1:p.Tyr168=
NM_004530.5:c.732C=	NP_004521.1:p.Tyr244=
ENST00000219070.8:c.732C=	ENSP00000219070.4:p.Tyr244=
ENST00000437642.6:c.582C=	ENSP00000394237.2:p.Tyr194=
ENST00000543485.5:c.504C=	ENSP00000444143.1:p.Tyr168=
ENST00000564864.5:c.504C=	ENSP00000456096.1:p.Tyr168=
ENST00000570308.5:c.504C=	ENSP00000461421.1:p.Tyr168=