Canonical Allele Identifier: CA2624150941
Gene: MMP14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843619A>C , CM000676.2:g.22843619A>C GRCh38
NC_000014.8:g.23312828A>C , CM000676.1:g.23312828A>C GRCh37
NC_000014.7:g.22382668A>C NCBI36
NG_046989.1:g.12087A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.851-91A>C MANE Select ENSP00000308208.6:n.851-91A>C
ENST00000548162.2:c.851-91A>C ENSP00000506068.1:n.851-91A>C
ENST00000680097.1:c.*166-91A>C ENSP00000506631.1:n.*166-91A>C
ENST00000680941.1:c.*249-91A>C ENSP00000506378.1:n.*249-91A>C
ENST00000311852.10:c.851-91A>C ENSP00000308208.6:n.851-91A>C
ENST00000548162.1:n.1093-91A>C
NM_004995.3:c.851-91A>C NP_004986.1:n.851-91A>C
NM_004995.4:c.851-91A>C MANE Select NP_004986.1:n.851-91A>C