Canonical Allele Identifier: CA1116331207
Gene: MMP16 HGNC NCBI

Linked Data

dbSNP Id: rs1808664384
gnomAD v3: 8-88077130-C-T
gnomAD v4: 8-88077130-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88077130C>T , CM000670.2:g.88077130C>T GRCh38
NC_000008.10:g.89089358C>T , CM000670.1:g.89089358C>T GRCh37
NC_000008.9:g.89158474C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286614.11:c.1084-2387G>A MANE Select ENSP00000286614.6:n.1084-2387G>A
ENST00000286614.10:c.1084-2387G>A ENSP00000286614.6:n.1084-2387G>A
ENST00000544227.5:n.1084-2387G>A
NM_005941.4:c.1084-2387G>A NP_005932.2:n.1084-2387G>A
XM_011517039.1:c.1084-2387G>A XP_011515341.1:n.1084-2387G>A
XM_011517040.1:c.1084-2387G>A XP_011515342.1:n.1084-2387G>A
XM_011517041.1:c.955-2387G>A XP_011515343.1:n.955-2387G>A
XM_011517042.1:c.1084-2387G>A XP_011515344.1:n.1084-2387G>A
XR_928334.1:n.1366-2387G>A
XM_024447154.1:c.295-2387G>A XP_024302922.1:n.295-2387G>A
NM_005941.5:c.1084-2387G>A MANE Select NP_005932.2:n.1084-2387G>A
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