Canonical Allele Identifier: CA2123185449

Gene: MMP14

Linked Data

• dbSNP Id: rs2039789091

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843604del , CM000676.2:g.22843604del	GRCh38
NC_000014.8:g.23312813del , CM000676.1:g.23312813del	GRCh37
NC_000014.7:g.22382653del	NCBI36
NG_046989.1:g.12072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.851-106del MANE Select	ENSP00000308208.6:n.851-106del
ENST00000548162.2:c.851-106del	ENSP00000506068.1:n.851-106del
ENST00000680097.1:c.*166-106del	ENSP00000506631.1:n.*166-106del
ENST00000680941.1:c.*249-106del	ENSP00000506378.1:n.*249-106del
ENST00000311852.10:c.851-106del	ENSP00000308208.6:n.851-106del
ENST00000548162.1:n.1093-106del
NM_004995.3:c.851-106del	NP_004986.1:n.851-106del
NM_004995.4:c.851-106del MANE Select	NP_004986.1:n.851-106del