Canonical Allele Identifier: CA2123185419
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843553T= , CM000676.2:g.22843553T= GRCh38
NC_000014.8:g.23312762T= , CM000676.1:g.23312762T= GRCh37
NC_000014.7:g.22382602T= NCBI36
NG_046989.1:g.12021T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.850+135T= MANE Select ENSP00000308208.6:n.850+135T=
ENST00000548162.2:c.850+135T= ENSP00000506068.1:n.850+135T=
ENST00000680097.1:c.*165+135T= ENSP00000506631.1:n.*165+135T=
ENST00000680941.1:c.*248+135T= ENSP00000506378.1:n.*248+135T=
ENST00000311852.10:c.850+135T= ENSP00000308208.6:n.850+135T=
ENST00000548162.1:n.1092+135T=
NM_004995.3:c.850+135T= NP_004986.1:n.850+135T=
NM_004995.4:c.850+135T= MANE Select NP_004986.1:n.850+135T=
Search 100 bp 5'
Search 100 bp 3'