Canonical Allele Identifier: CA485592363
Gene: MMP14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23313642C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22844433C>A , CM000676.2:g.22844433C>A GRCh38
NC_000014.8:g.23313642C>A , CM000676.1:g.23313642C>A GRCh37
NC_000014.7:g.22383482C>A NCBI36
NG_046989.1:g.12901C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311852.11:c.1074C>A MANE Select ENSP00000308208.6:p.Gly358=
ENST00000548162.2:c.1074C>A ENSP00000506068.1:p.Gly358=
ENST00000680097.1:c.*389C>A ENSP00000506631.1:n.*389C>A
ENST00000680941.1:c.*472C>A ENSP00000506378.1:n.*472C>A
ENST00000311852.10:c.1074C>A ENSP00000308208.6:p.Gly358=
ENST00000548162.1:n.1316C>A
NM_004995.3:c.1074C>A NP_004986.1:p.Gly358=
NM_004995.4:c.1074C>A MANE Select NP_004986.1:p.Gly358=
Search 100 bp 5'
Search 100 bp 3'