Canonical Allele Identifier: CA1800556672

Gene: MMP16

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88060856A>C , CM000670.2:g.88060856A>C	GRCh38
NC_000008.10:g.89073084A>C , CM000670.1:g.89073084A>C	GRCh37
NC_000008.9:g.89142200A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286614.11:c.1223-4578T>G MANE Select	ENSP00000286614.6:n.1223-4578T>G
ENST00000286614.10:c.1223-4578T>G	ENSP00000286614.6:n.1223-4578T>G
NM_005941.4:c.1223-4578T>G	NP_005932.2:n.1223-4578T>G
XM_011517039.1:c.1223-4578T>G	XP_011515341.1:n.1223-4578T>G
XM_011517040.1:c.1223-4578T>G	XP_011515342.1:n.1223-4578T>G
XM_011517041.1:c.1094-4578T>G	XP_011515343.1:n.1094-4578T>G
XR_928334.1:n.1505-4578T>G
XM_024447154.1:c.434-4578T>G	XP_024302922.1:n.434-4578T>G
NM_005941.5:c.1223-4578T>G MANE Select	NP_005932.2:n.1223-4578T>G