Canonical Allele Identifier: CA257746196
Gene: MMP14 HGNC NCBI

Linked Data

dbSNP Id: rs1026028199
MyVariant Identifiers: chr14:g.23312390A>C (hg19) chr14:g.22843181A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843181A>C , CM000676.2:g.22843181A>C GRCh38
NC_000014.8:g.23312390A>C , CM000676.1:g.23312390A>C GRCh37
NC_000014.7:g.22382230A>C NCBI36
NG_046989.1:g.11649A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-76A>C MANE Select ENSP00000308208.6:n.689-76A>C
ENST00000548162.2:c.689-76A>C ENSP00000506068.1:n.689-76A>C
ENST00000680097.1:c.*4-76A>C ENSP00000506631.1:n.*4-76A>C
ENST00000680941.1:c.*86+9A>C ENSP00000506378.1:n.*86+9A>C
ENST00000311852.10:c.689-76A>C ENSP00000308208.6:n.689-76A>C
ENST00000548162.1:n.931-76A>C
NM_004995.3:c.689-76A>C NP_004986.1:n.689-76A>C
NM_004995.4:c.689-76A>C MANE Select NP_004986.1:n.689-76A>C
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