Canonical Allele Identifier: CA2123185381
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843488T= , CM000676.2:g.22843488T= GRCh38
NC_000014.8:g.23312697T= , CM000676.1:g.23312697T= GRCh37
NC_000014.7:g.22382537T= NCBI36
NG_046989.1:g.11956T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.850+70T= MANE Select ENSP00000308208.6:n.850+70T=
ENST00000548162.2:c.850+70T= ENSP00000506068.1:n.850+70T=
ENST00000680097.1:c.*165+70T= ENSP00000506631.1:n.*165+70T=
ENST00000680941.1:c.*248+70T= ENSP00000506378.1:n.*248+70T=
ENST00000311852.10:c.850+70T= ENSP00000308208.6:n.850+70T=
ENST00000548162.1:n.1092+70T=
NM_004995.3:c.850+70T= NP_004986.1:n.850+70T=
NM_004995.4:c.850+70T= MANE Select NP_004986.1:n.850+70T=
Search 100 bp 5'
Search 100 bp 3'