Canonical Allele Identifier: CA2633277227

Gene: MMP2

Linked Data

• gnomAD v4: 16-55482922-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55482925_55482927del , CM000678.2:g.55482925_55482927del	GRCh38
NC_000016.9:g.55516837_55516839del , CM000678.1:g.55516837_55516839del	GRCh37
NC_000016.8:g.54074338_54074340del	NCBI36
NG_008989.1:g.8757_8759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219070.9:c.170_172del MANE Select	ENSP00000219070.4:p.Phe57del
ENST00000219070.8:c.170_172del	ENSP00000219070.4:p.Phe57del
ENST00000437642.6:c.20_22del	ENSP00000394237.2:p.Phe7del
ENST00000543485.5:c.-59_-57del	ENSP00000444143.1:n.-59_-57del
ENST00000564864.5:c.-59_-57del	ENSP00000456096.1:n.-59_-57del
ENST00000568715.5:c.-59_-57del	ENSP00000457949.1:n.-59_-57del
ENST00000570308.5:c.-59_-57del	ENSP00000461421.1:n.-59_-57del
NM_001127891.2:c.20_22del	NP_001121363.1:p.Phe7del
NM_001302508.1:c.-59_-57del	NP_001289437.1:n.-59_-57del
NM_001302509.1:c.-59_-57del	NP_001289438.1:n.-59_-57del
NM_001302510.1:c.-59_-57del	NP_001289439.1:n.-59_-57del
NM_004530.5:c.170_172del	NP_004521.1:p.Phe57del
NM_004530.6:c.170_172del MANE Select	NP_004521.1:p.Phe57del
NM_001127891.3:c.20_22del	NP_001121363.1:p.Phe7del
NM_001302509.2:c.-59_-57del	NP_001289438.1:n.-59_-57del
NM_001302510.2:c.-59_-57del	NP_001289439.1:n.-59_-57del