Canonical Allele Identifier: CA2800858646
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843196del , CM000676.2:g.22843196del GRCh38
NC_000014.8:g.23312405del , CM000676.1:g.23312405del GRCh37
NC_000014.7:g.22382245del NCBI36
NG_046989.1:g.11664del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-61del MANE Select ENSP00000308208.6:n.689-61del
ENST00000548162.2:c.689-61del ENSP00000506068.1:n.689-61del
ENST00000680097.1:c.*4-61del ENSP00000506631.1:n.*4-61del
ENST00000680941.1:c.*86+24del ENSP00000506378.1:n.*86+24del
ENST00000311852.10:c.689-61del ENSP00000308208.6:n.689-61del
ENST00000548162.1:n.931-61del
NM_004995.3:c.689-61del NP_004986.1:n.689-61del
NM_004995.4:c.689-61del MANE Select NP_004986.1:n.689-61del