Canonical Allele Identifier: CA6881786

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131840769G>A , CM000674.2:g.131840769G>A	GRCh38
NC_000012.11:g.132325314G>A , CM000674.1:g.132325314G>A	GRCh37
NC_000012.10:g.130891267G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.619G>A	ENSP00000445620.2:p.Val207Met
ENST00000545671.6:c.*306G>A	ENSP00000444603.2:n.*306G>A
ENST00000545790.6:c.619G>A	ENSP00000441710.2:p.Val207Met
ENST00000360564.5:c.619G>A MANE Select	ENSP00000353767.1:p.Val207Met
ENST00000534865.1:c.142G>A	ENSP00000442104.1:p.Val48Met
ENST00000535182.1:n.34G>A
ENST00000535291.5:c.367G>A	ENSP00000441106.1:p.Val123Met
ENST00000545671.5:c.307G>A	ENSP00000444603.1:p.Val103Met
NM_016155.4:c.619G>A	NP_057239.4:p.Val207Met
XM_011538355.1:c.367G>A	XP_011536657.1:p.Val123Met
XM_011538356.1:c.367G>A	XP_011536658.1:p.Val123Met
XM_011538357.1:c.367G>A	XP_011536659.1:p.Val123Met
XR_944550.1:n.707G>A
XR_944551.1:n.707G>A
XR_944552.1:n.707G>A
NM_016155.6:c.619G>A	NP_057239.4:p.Val207Met
XM_011538355.3:c.367G>A	XP_011536657.1:p.Val123Met
XM_011538356.3:c.367G>A	XP_011536658.1:p.Val123Met
XM_011538357.2:c.367G>A	XP_011536659.1:p.Val123Met
XM_017019307.1:c.619G>A	XP_016874796.1:p.Val207Met
XR_001748705.1:n.700G>A
XR_944550.2:n.700G>A
XR_944551.2:n.700G>A
XR_944552.2:n.700G>A
NM_016155.7:c.619G>A MANE Select	NP_057239.4:p.Val207Met