Canonical Allele Identifier: CA388931176
Gene: MMP14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23312626T>A (hg19) chr14:g.22843417T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843417T>A , CM000676.2:g.22843417T>A GRCh38
NC_000014.8:g.23312626T>A , CM000676.1:g.23312626T>A GRCh37
NC_000014.7:g.22382466T>A NCBI36
NG_046989.1:g.11885T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.849T>A MANE Select ENSP00000308208.6:p.Tyr283Ter
ENST00000548162.2:c.849T>A ENSP00000506068.1:p.Tyr283Ter
ENST00000680097.1:c.*164T>A ENSP00000506631.1:n.*164T>A
ENST00000680941.1:c.*247T>A ENSP00000506378.1:n.*247T>A
ENST00000311852.10:c.849T>A ENSP00000308208.6:p.Tyr283Ter
ENST00000548162.1:n.1091T>A
NM_004995.3:c.849T>A NP_004986.1:p.Tyr283Ter
NM_004995.4:c.849T>A MANE Select NP_004986.1:p.Tyr283Ter
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