Canonical Allele Identifier: CA6881728

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131840614C>T , CM000674.2:g.131840614C>T	GRCh38
NC_000012.11:g.132325159C>T , CM000674.1:g.132325159C>T	GRCh37
NC_000012.10:g.130891112C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.464C>T	ENSP00000445620.2:p.Thr155Met
ENST00000545671.6:c.*151C>T	ENSP00000444603.2:n.*151C>T
ENST00000545790.6:c.464C>T	ENSP00000441710.2:p.Thr155Met
ENST00000360564.5:c.464C>T MANE Select	ENSP00000353767.1:p.Thr155Met
ENST00000534865.1:c.-14C>T	ENSP00000442104.1:n.-14C>T
ENST00000535291.5:c.212C>T	ENSP00000441106.1:p.Thr71Met
ENST00000545671.5:c.152C>T	ENSP00000444603.1:p.Thr51Met
ENST00000545790.5:c.212C>T	ENSP00000441710.1:p.Thr71Met
NM_016155.4:c.464C>T	NP_057239.4:p.Thr155Met
XM_011538355.1:c.212C>T	XP_011536657.1:p.Thr71Met
XM_011538356.1:c.212C>T	XP_011536658.1:p.Thr71Met
XM_011538357.1:c.212C>T	XP_011536659.1:p.Thr71Met
XR_944550.1:n.552C>T
XR_944551.1:n.552C>T
XR_944552.1:n.552C>T
NM_016155.6:c.464C>T	NP_057239.4:p.Thr155Met
XM_011538355.3:c.212C>T	XP_011536657.1:p.Thr71Met
XM_011538356.3:c.212C>T	XP_011536658.1:p.Thr71Met
XM_011538357.2:c.212C>T	XP_011536659.1:p.Thr71Met
XM_017019307.1:c.464C>T	XP_016874796.1:p.Thr155Met
XR_001748705.1:n.545C>T
XR_944550.2:n.545C>T
XR_944551.2:n.545C>T
XR_944552.2:n.545C>T
NM_016155.7:c.464C>T MANE Select	NP_057239.4:p.Thr155Met