Canonical Allele Identifier: CA2123185238
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843112A= , CM000676.2:g.22843112A= GRCh38
NC_000014.8:g.23312321A= , CM000676.1:g.23312321A= GRCh37
NC_000014.7:g.22382161A= NCBI36
NG_046989.1:g.11580A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-145A= MANE Select ENSP00000308208.6:n.689-145A=
ENST00000548162.2:c.689-145A= ENSP00000506068.1:n.689-145A=
ENST00000680097.1:c.*4-145A= ENSP00000506631.1:n.*4-145A=
ENST00000680941.1:c.*26A= ENSP00000506378.1:n.*26A=
ENST00000311852.10:c.689-145A= ENSP00000308208.6:n.689-145A=
ENST00000548162.1:n.931-145A=
NM_004995.3:c.689-145A= NP_004986.1:n.689-145A=
NM_004995.4:c.689-145A= MANE Select NP_004986.1:n.689-145A=