Canonical Allele Identifier: CA2123185458
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843633A= , CM000676.2:g.22843633A= GRCh38
NC_000014.8:g.23312842A= , CM000676.1:g.23312842A= GRCh37
NC_000014.7:g.22382682A= NCBI36
NG_046989.1:g.12101A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311852.11:c.851-77A= MANE Select ENSP00000308208.6:n.851-77A=
ENST00000548162.2:c.851-77A= ENSP00000506068.1:n.851-77A=
ENST00000680097.1:c.*166-77A= ENSP00000506631.1:n.*166-77A=
ENST00000680941.1:c.*249-77A= ENSP00000506378.1:n.*249-77A=
ENST00000311852.10:c.851-77A= ENSP00000308208.6:n.851-77A=
ENST00000548162.1:n.1093-77A=
NM_004995.3:c.851-77A= NP_004986.1:n.851-77A=
NM_004995.4:c.851-77A= MANE Select NP_004986.1:n.851-77A=
Search 100 bp 5'
Search 100 bp 3'