Canonical Allele Identifier: CA6881725

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131840613A>T , CM000674.2:g.131840613A>T	GRCh38
NC_000012.11:g.132325158A>T , CM000674.1:g.132325158A>T	GRCh37
NC_000012.10:g.130891111A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.463A>T	ENSP00000445620.2:p.Thr155Ser
ENST00000545671.6:c.*150A>T	ENSP00000444603.2:n.*150A>T
ENST00000545790.6:c.463A>T	ENSP00000441710.2:p.Thr155Ser
ENST00000360564.5:c.463A>T MANE Select	ENSP00000353767.1:p.Thr155Ser
ENST00000534865.1:c.-15A>T	ENSP00000442104.1:n.-15A>T
ENST00000535291.5:c.211A>T	ENSP00000441106.1:p.Thr71Ser
ENST00000545671.5:c.151A>T	ENSP00000444603.1:p.Thr51Ser
ENST00000545790.5:c.211A>T	ENSP00000441710.1:p.Thr71Ser
NM_016155.4:c.463A>T	NP_057239.4:p.Thr155Ser
XM_011538355.1:c.211A>T	XP_011536657.1:p.Thr71Ser
XM_011538356.1:c.211A>T	XP_011536658.1:p.Thr71Ser
XM_011538357.1:c.211A>T	XP_011536659.1:p.Thr71Ser
XR_944550.1:n.551A>T
XR_944551.1:n.551A>T
XR_944552.1:n.551A>T
NM_016155.6:c.463A>T	NP_057239.4:p.Thr155Ser
XM_011538355.3:c.211A>T	XP_011536657.1:p.Thr71Ser
XM_011538356.3:c.211A>T	XP_011536658.1:p.Thr71Ser
XM_011538357.2:c.211A>T	XP_011536659.1:p.Thr71Ser
XM_017019307.1:c.463A>T	XP_016874796.1:p.Thr155Ser
XR_001748705.1:n.544A>T
XR_944550.2:n.544A>T
XR_944551.2:n.544A>T
XR_944552.2:n.544A>T
NM_016155.7:c.463A>T MANE Select	NP_057239.4:p.Thr155Ser