Canonical Allele Identifier: CA387284547

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131838255A>G , CM000674.2:g.131838255A>G	GRCh38
NC_000012.11:g.132322800A>G , CM000674.1:g.132322800A>G	GRCh37
NC_000012.10:g.130888753A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.220A>G	ENSP00000445620.2:p.Thr74Ala
ENST00000545671.6:c.160-357A>G	ENSP00000444603.2:n.160-357A>G
ENST00000545790.6:c.220A>G	ENSP00000441710.2:p.Thr74Ala
ENST00000360564.5:c.220A>G MANE Select	ENSP00000353767.1:p.Thr74Ala
ENST00000535291.5:c.-33A>G	ENSP00000441106.1:n.-33A>G
ENST00000545671.5:c.-20-357A>G	ENSP00000444603.1:n.-20-357A>G
ENST00000545790.5:c.-33A>G	ENSP00000441710.1:n.-33A>G
NM_016155.4:c.220A>G	NP_057239.4:p.Thr74Ala
XM_011538355.1:c.-33A>G	XP_011536657.1:n.-33A>G
XM_011538356.1:c.-33A>G	XP_011536658.1:n.-33A>G
XM_011538357.1:c.-33A>G	XP_011536659.1:n.-33A>G
XR_944550.1:n.308A>G
XR_944551.1:n.308A>G
XR_944552.1:n.308A>G
NM_016155.6:c.220A>G	NP_057239.4:p.Thr74Ala
XM_011538355.3:c.-33A>G	XP_011536657.1:n.-33A>G
XM_011538356.3:c.-33A>G	XP_011536658.1:n.-33A>G
XM_011538357.2:c.-33A>G	XP_011536659.1:n.-33A>G
XM_017019307.1:c.220A>G	XP_016874796.1:p.Thr74Ala
XR_001748705.1:n.301A>G
XR_944550.2:n.301A>G
XR_944551.2:n.301A>G
XR_944552.2:n.301A>G
NM_016155.7:c.220A>G MANE Select	NP_057239.4:p.Thr74Ala