Canonical Allele Identifier: CA257746143
Gene: MMP14 HGNC NCBI

Linked Data

dbSNP Id: rs17885327
gnomAD v2: 14-23312308-T-C
gnomAD v3: 14-22843099-T-C
gnomAD v4: 14-22843099-T-C
MyVariant Identifiers: chr14:g.23312308T>C (hg19) chr14:g.22843099T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843099T>C , CM000676.2:g.22843099T>C GRCh38
NC_000014.8:g.23312308T>C , CM000676.1:g.23312308T>C GRCh37
NC_000014.7:g.22382148T>C NCBI36
NG_046989.1:g.11567T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-158T>C MANE Select ENSP00000308208.6:n.689-158T>C
ENST00000548162.2:c.689-158T>C ENSP00000506068.1:n.689-158T>C
ENST00000680097.1:c.*4-158T>C ENSP00000506631.1:n.*4-158T>C
ENST00000680941.1:c.*13T>C ENSP00000506378.1:n.*13T>C
ENST00000311852.10:c.689-158T>C ENSP00000308208.6:n.689-158T>C
ENST00000548162.1:n.931-158T>C
NM_004995.3:c.689-158T>C NP_004986.1:n.689-158T>C
NM_004995.4:c.689-158T>C MANE Select NP_004986.1:n.689-158T>C
Search 100 bp 5'
Search 100 bp 3'