Canonical Allele Identifier: CA2123185852
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22844358G= , CM000676.2:g.22844358G= GRCh38
NC_000014.8:g.23313567G= , CM000676.1:g.23313567G= GRCh37
NC_000014.7:g.22383407G= NCBI36
NG_046989.1:g.12826G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311852.11:c.1012-13G= MANE Select ENSP00000308208.6:n.1012-13G=
ENST00000548162.2:c.1012-13G= ENSP00000506068.1:n.1012-13G=
ENST00000680097.1:c.*327-13G= ENSP00000506631.1:n.*327-13G=
ENST00000680941.1:c.*410-13G= ENSP00000506378.1:n.*410-13G=
ENST00000311852.10:c.1012-13G= ENSP00000308208.6:n.1012-13G=
ENST00000548162.1:n.1254-13G=
NM_004995.3:c.1012-13G= NP_004986.1:n.1012-13G=
NM_004995.4:c.1012-13G= MANE Select NP_004986.1:n.1012-13G=
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