Canonical Allele Identifier: CA2123185228
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843089_22843096delinsGGCTTTGT , CM000676.2:g.22843089_22843096delinsGGCTTTGT GRCh38
NC_000014.8:g.23312298_23312305delinsGGCTTTGT , CM000676.1:g.23312298_23312305delinsGGCTTTGT GRCh37
NC_000014.7:g.22382138_22382145delinsGGCTTTGT NCBI36
NG_046989.1:g.11557_11564delinsGGCTTTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-168_689-161delinsGGCTTTGT MANE Select ENSP00000308208.6:n.689-168_689-161delinsGGCTTTGT
ENST00000548162.2:c.689-168_689-161delinsGGCTTTGT ENSP00000506068.1:n.689-168_689-161delinsGGCTTTGT
ENST00000680097.1:c.*4-168_*4-161delinsGGCTTTGT ENSP00000506631.1:n.*4-168_*4-161delinsGGCTTTGT
ENST00000680941.1:c.*3_*10delinsGGCTTTGT ENSP00000506378.1:n.*3_*10delinsGGCTTTGT
ENST00000311852.10:c.689-168_689-161delinsGGCTTTGT ENSP00000308208.6:n.689-168_689-161delinsGGCTTTGT
ENST00000548162.1:n.931-168_931-161delinsGGCTTTGT
NM_004995.3:c.689-168_689-161delinsGGCTTTGT NP_004986.1:n.689-168_689-161delinsGGCTTTGT
NM_004995.4:c.689-168_689-161delinsGGCTTTGT MANE Select NP_004986.1:n.689-168_689-161delinsGGCTTTGT