Canonical Allele Identifier: CA388931131
Gene: MMP14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843395G>C , CM000676.2:g.22843395G>C GRCh38
NC_000014.8:g.23312604G>C , CM000676.1:g.23312604G>C GRCh37
NC_000014.7:g.22382444G>C NCBI36
NG_046989.1:g.11863G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.827G>C MANE Select ENSP00000308208.6:p.Arg276Pro
ENST00000548162.2:c.827G>C ENSP00000506068.1:p.Arg276Pro
ENST00000680097.1:c.*142G>C ENSP00000506631.1:n.*142G>C
ENST00000680941.1:c.*225G>C ENSP00000506378.1:n.*225G>C
ENST00000311852.10:c.827G>C ENSP00000308208.6:p.Arg276Pro
ENST00000548162.1:n.1069G>C
NM_004995.3:c.827G>C NP_004986.1:p.Arg276Pro
NM_004995.4:c.827G>C MANE Select NP_004986.1:p.Arg276Pro