Canonical Allele Identifier: CA2123185234
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843100_22843101delinsTA , CM000676.2:g.22843100_22843101delinsTA GRCh38
NC_000014.8:g.23312309_23312310delinsTA , CM000676.1:g.23312309_23312310delinsTA GRCh37
NC_000014.7:g.22382149_22382150delinsTA NCBI36
NG_046989.1:g.11568_11569delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-157_689-156delinsTA MANE Select ENSP00000308208.6:n.689-157_689-156delinsTA
ENST00000548162.2:c.689-157_689-156delinsTA ENSP00000506068.1:n.689-157_689-156delinsTA
ENST00000680097.1:c.*4-157_*4-156delinsTA ENSP00000506631.1:n.*4-157_*4-156delinsTA
ENST00000680941.1:c.*14_*15delinsTA ENSP00000506378.1:n.*14_*15delinsTA
ENST00000311852.10:c.689-157_689-156delinsTA ENSP00000308208.6:n.689-157_689-156delinsTA
ENST00000548162.1:n.931-157_931-156delinsTA
NM_004995.3:c.689-157_689-156delinsTA NP_004986.1:n.689-157_689-156delinsTA
NM_004995.4:c.689-157_689-156delinsTA MANE Select NP_004986.1:n.689-157_689-156delinsTA