Canonical Allele Identifier: CA485591330
Gene: MMP14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23312605C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843396C>A , CM000676.2:g.22843396C>A GRCh38
NC_000014.8:g.23312605C>A , CM000676.1:g.23312605C>A GRCh37
NC_000014.7:g.22382445C>A NCBI36
NG_046989.1:g.11864C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.828C>A MANE Select ENSP00000308208.6:p.Arg276=
ENST00000548162.2:c.828C>A ENSP00000506068.1:p.Arg276=
ENST00000680097.1:c.*143C>A ENSP00000506631.1:n.*143C>A
ENST00000680941.1:c.*226C>A ENSP00000506378.1:n.*226C>A
ENST00000311852.10:c.828C>A ENSP00000308208.6:p.Arg276=
ENST00000548162.1:n.1070C>A
NM_004995.3:c.828C>A NP_004986.1:p.Arg276=
NM_004995.4:c.828C>A MANE Select NP_004986.1:p.Arg276=
Search 100 bp 5'
Search 100 bp 3'