Canonical Allele Identifier: CA6881799

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131840824A>T , CM000674.2:g.131840824A>T	GRCh38
NC_000012.11:g.132325369A>T , CM000674.1:g.132325369A>T	GRCh37
NC_000012.10:g.130891322A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.674A>T	ENSP00000445620.2:p.Asp225Val
ENST00000545671.6:c.*361A>T	ENSP00000444603.2:n.*361A>T
ENST00000545790.6:c.674A>T	ENSP00000441710.2:p.Asp225Val
ENST00000360564.5:c.674A>T MANE Select	ENSP00000353767.1:p.Asp225Val
ENST00000534865.1:c.197A>T	ENSP00000442104.1:p.Asp66Val
ENST00000535182.1:n.89A>T
ENST00000535291.5:c.422A>T	ENSP00000441106.1:p.Asp141Val
ENST00000545671.5:c.362A>T	ENSP00000444603.1:p.Asp121Val
NM_016155.4:c.674A>T	NP_057239.4:p.Asp225Val
XM_011538355.1:c.422A>T	XP_011536657.1:p.Asp141Val
XM_011538356.1:c.422A>T	XP_011536658.1:p.Asp141Val
XM_011538357.1:c.422A>T	XP_011536659.1:p.Asp141Val
XR_944550.1:n.762A>T
XR_944551.1:n.762A>T
XR_944552.1:n.762A>T
NM_016155.6:c.674A>T	NP_057239.4:p.Asp225Val
XM_011538355.3:c.422A>T	XP_011536657.1:p.Asp141Val
XM_011538356.3:c.422A>T	XP_011536658.1:p.Asp141Val
XM_011538357.2:c.422A>T	XP_011536659.1:p.Asp141Val
XM_017019307.1:c.674A>T	XP_016874796.1:p.Asp225Val
XR_001748705.1:n.755A>T
XR_944550.2:n.755A>T
XR_944551.2:n.755A>T
XR_944552.2:n.755A>T
NM_016155.7:c.674A>T MANE Select	NP_057239.4:p.Asp225Val