Canonical Allele Identifier: CA485591120
Gene: MMP14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23312488T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843279T>A , CM000676.2:g.22843279T>A GRCh38
NC_000014.8:g.23312488T>A , CM000676.1:g.23312488T>A GRCh37
NC_000014.7:g.22382328T>A NCBI36
NG_046989.1:g.11747T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.711T>A MANE Select ENSP00000308208.6:p.Ala237=
ENST00000548162.2:c.711T>A ENSP00000506068.1:p.Ala237=
ENST00000680097.1:c.*26T>A ENSP00000506631.1:n.*26T>A
ENST00000680941.1:c.*109T>A ENSP00000506378.1:n.*109T>A
ENST00000311852.10:c.711T>A ENSP00000308208.6:p.Ala237=
ENST00000548162.1:n.953T>A
NM_004995.3:c.711T>A NP_004986.1:p.Ala237=
NM_004995.4:c.711T>A MANE Select NP_004986.1:p.Ala237=
Search 100 bp 5'
Search 100 bp 3'