Canonical Allele Identifier: CA2397953014
Gene: MMP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23775729A>T , CM000684.2:g.23775729A>T GRCh38
NC_000022.10:g.24117916A>T , CM000684.1:g.24117916A>T GRCh37
NC_000022.9:g.22447916A>T NCBI36
NG_029443.1:g.7881A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215743.8:c.108+2751A>T MANE Select ENSP00000215743.3:n.108+2751A>T
ENST00000215743.7:c.108+2751A>T ENSP00000215743.3:n.108+2751A>T
ENST00000428253.1:c.108+2751A>T ENSP00000409860.1:n.108+2751A>T
ENST00000437086.5:c.108+2751A>T ENSP00000408070.1:n.108+2751A>T
ENST00000465385.5:n.751-3458A>T
ENST00000465730.1:n.133+2751A>T
ENST00000477567.5:n.273-3458A>T
ENST00000489582.5:n.135-3458A>T
NM_005940.3:c.108+2751A>T NP_005931.2:n.108+2751A>T
NM_005940.4:c.108+2751A>T NP_005931.2:n.108+2751A>T
NR_133013.1:n.160+2751A>T
NM_005940.5:c.108+2751A>T MANE Select NP_005931.2:n.108+2751A>T
NR_133013.2:n.130+2751A>T