Canonical Allele Identifier: CA485592345
Gene: MMP14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23313639T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22844430T>A , CM000676.2:g.22844430T>A GRCh38
NC_000014.8:g.23313639T>A , CM000676.1:g.23313639T>A GRCh37
NC_000014.7:g.22383479T>A NCBI36
NG_046989.1:g.12898T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311852.11:c.1071T>A MANE Select ENSP00000308208.6:p.Ile357=
ENST00000548162.2:c.1071T>A ENSP00000506068.1:p.Ile357=
ENST00000680097.1:c.*386T>A ENSP00000506631.1:n.*386T>A
ENST00000680941.1:c.*469T>A ENSP00000506378.1:n.*469T>A
ENST00000311852.10:c.1071T>A ENSP00000308208.6:p.Ile357=
ENST00000548162.1:n.1313T>A
NM_004995.3:c.1071T>A NP_004986.1:p.Ile357=
NM_004995.4:c.1071T>A MANE Select NP_004986.1:p.Ile357=
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