Canonical Allele Identifier: CA2123185428
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843562_22843564delinsCAT , CM000676.2:g.22843562_22843564delinsCAT GRCh38
NC_000014.8:g.23312771_23312773delinsCAT , CM000676.1:g.23312771_23312773delinsCAT GRCh37
NC_000014.7:g.22382611_22382613delinsCAT NCBI36
NG_046989.1:g.12030_12032delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.850+144_851-146delinsCAT MANE Select ENSP00000308208.6:n.850+144_851-146delinsCAT
ENST00000548162.2:c.850+144_851-146delinsCAT ENSP00000506068.1:n.850+144_851-146delinsCAT
ENST00000680097.1:c.*165+144_*166-146delinsCAT ENSP00000506631.1:n.*165+144_*166-146delinsCAT
ENST00000680941.1:c.*248+144_*249-146delinsCAT ENSP00000506378.1:n.*248+144_*249-146delinsCAT
ENST00000311852.10:c.850+144_851-146delinsCAT ENSP00000308208.6:n.850+144_851-146delinsCAT
ENST00000548162.1:n.1092+144_1093-146delinsCAT
NM_004995.3:c.850+144_851-146delinsCAT NP_004986.1:n.850+144_851-146delinsCAT
NM_004995.4:c.850+144_851-146delinsCAT MANE Select NP_004986.1:n.850+144_851-146delinsCAT