Canonical Allele Identifier: CA2838418656
Gene: MMP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23782186G>T , CM000684.2:g.23782186G>T GRCh38
NC_000022.10:g.24124373G>T , CM000684.1:g.24124373G>T GRCh37
NC_000022.9:g.22454373G>T NCBI36
NG_009303.1:g.224G>T , LRG_520:g.224G>T
NG_029443.1:g.14338G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215743.8:c.1076-40G>T MANE Select ENSP00000215743.3:n.1076-40G>T
ENST00000215743.7:c.1076-40G>T ENSP00000215743.3:n.1076-40G>T
ENST00000434318.1:c.837G>T
ENST00000437086.5:c.1028-182G>T ENSP00000408070.1:n.1028-182G>T
ENST00000465385.5:n.2660-40G>T
ENST00000480185.1:n.113-40G>T
ENST00000488363.1:n.147-40G>T
ENST00000493132.1:n.470-40G>T
NM_005940.3:c.1076-40G>T NP_005931.2:n.1076-40G>T
NM_005940.4:c.1076-40G>T NP_005931.2:n.1076-40G>T
NR_133013.1:n.1080-182G>T
NM_005940.5:c.1076-40G>T MANE Select NP_005931.2:n.1076-40G>T
NR_133013.2:n.1050-182G>T