Canonical Allele Identifier: CA388930969
Gene: MMP14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23312532A>C (hg19) chr14:g.22843323A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843323A>C , CM000676.2:g.22843323A>C GRCh38
NC_000014.8:g.23312532A>C , CM000676.1:g.23312532A>C GRCh37
NC_000014.7:g.22382372A>C NCBI36
NG_046989.1:g.11791A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.755A>C MANE Select ENSP00000308208.6:p.Asp252Ala
ENST00000548162.2:c.755A>C ENSP00000506068.1:p.Asp252Ala
ENST00000680097.1:c.*70A>C ENSP00000506631.1:n.*70A>C
ENST00000680941.1:c.*153A>C ENSP00000506378.1:n.*153A>C
ENST00000311852.10:c.755A>C ENSP00000308208.6:p.Asp252Ala
ENST00000548162.1:n.997A>C
NM_004995.3:c.755A>C NP_004986.1:p.Asp252Ala
NM_004995.4:c.755A>C MANE Select NP_004986.1:p.Asp252Ala
Search 100 bp 5'
Search 100 bp 3'