Canonical Allele Identifier: CA257746144
Gene: MMP14 HGNC NCBI

Linked Data

dbSNP Id: rs966473551
gnomAD v2: 14-23312309-TA-T
gnomAD v3: 14-22843100-TA-T
gnomAD v4: 14-22843100-TA-T
MyVariant Identifiers: chr14:g.23312310del (hg19) chr14:g.22843101del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843103del , CM000676.2:g.22843103del GRCh38
NC_000014.8:g.23312312del , CM000676.1:g.23312312del GRCh37
NC_000014.7:g.22382152del NCBI36
NG_046989.1:g.11571del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-154del MANE Select ENSP00000308208.6:n.689-154del
ENST00000548162.2:c.689-154del ENSP00000506068.1:n.689-154del
ENST00000680097.1:c.*4-154del ENSP00000506631.1:n.*4-154del
ENST00000680941.1:c.*17del ENSP00000506378.1:n.*17del
ENST00000311852.10:c.689-154del ENSP00000308208.6:n.689-154del
ENST00000548162.1:n.931-154del
NM_004995.3:c.689-154del NP_004986.1:n.689-154del
NM_004995.4:c.689-154del MANE Select NP_004986.1:n.689-154del
Search 100 bp 5'
Search 100 bp 3'