Canonical Allele Identifier: CA271895

Gene: MTM1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641289G>A , CM000685.2:g.150641289G>A	GRCh38
NC_000023.10:g.149809762G>A , CM000685.1:g.149809762G>A	GRCh37
NC_000023.9:g.149560420G>A	NCBI36
NG_008199.1:g.77716G>A , LRG_839:g.77716G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*82G>A	ENSP00000509844.1:n.*82G>A
ENST00000685439.1:c.204G>A	ENSP00000508454.1:p.Trp68Ter
ENST00000685944.1:c.549G>A	ENSP00000509266.1:p.Trp183Ter
ENST00000686212.1:n.151G>A
ENST00000687215.1:c.*304G>A	ENSP00000509706.1:n.*304G>A
ENST00000688152.1:c.605G>A	ENSP00000509360.1:p.Gly202Glu
ENST00000688403.1:c.-196G>A	ENSP00000508944.1:n.-196G>A
ENST00000689314.1:c.594G>A	ENSP00000510607.1:p.Trp198Ter
ENST00000689694.1:c.549G>A	ENSP00000508718.1:p.Trp183Ter
ENST00000689810.1:c.*198G>A	ENSP00000510635.1:n.*198G>A
ENST00000690282.1:c.-196G>A	ENSP00000509809.1:n.-196G>A
ENST00000690351.1:c.*201G>A	ENSP00000509728.1:n.*201G>A
ENST00000691232.1:c.204G>A	ENSP00000509675.1:p.Trp68Ter
ENST00000691482.1:n.1564G>A
ENST00000691686.1:c.549G>A	ENSP00000509784.1:p.Trp183Ter
ENST00000691851.1:c.549G>A	ENSP00000510106.1:p.Trp183Ter
ENST00000692015.1:c.336G>A	ENSP00000510634.1:p.Trp112Ter
ENST00000692638.1:c.*354G>A	ENSP00000509412.1:n.*354G>A
ENST00000692852.1:c.549G>A	ENSP00000510337.1:p.Trp183Ter
ENST00000692915.1:c.*756G>A	ENSP00000508547.1:n.*756G>A
ENST00000370396.7:c.549G>A MANE Select	ENSP00000359423.3:p.Trp183Ter
ENST00000306167.11:n.416G>A
ENST00000370396.6:c.549G>A	ENSP00000359423.2:p.Trp183Ter
ENST00000490530.1:n.488G>A
NM_000252.2:c.549G>A , LRG_839t1:c.549G>A	NP_000243.1:p.Trp183Ter
XM_005274687.2:c.549G>A	XP_005274744.1:p.Trp183Ter
XM_011531170.1:c.615G>A	XP_011529472.1:p.Trp205Ter
XM_011531171.1:c.594G>A	XP_011529473.1:p.Trp198Ter
XM_011531172.1:c.594G>A	XP_011529474.1:p.Trp198Ter
XM_011531173.1:c.549G>A	XP_011529475.1:p.Trp183Ter
XM_011531173.2:c.549G>A	XP_011529475.1:p.Trp183Ter
XM_017029547.1:c.594G>A	XP_016885036.1:p.Trp198Ter
XM_017029548.1:c.594G>A	XP_016885037.1:p.Trp198Ter
XM_017029549.1:c.549G>A	XP_016885038.1:p.Trp183Ter
XM_017029550.1:c.438G>A	XP_016885039.1:p.Trp146Ter
XM_017029551.2:c.-196G>A	XP_016885040.1:n.-196G>A
NM_000252.3:c.549G>A MANE Select	NP_000243.1:p.Trp183Ter
NM_001376906.1:c.549G>A	NP_001363835.1:p.Trp183Ter
NM_001376907.1:c.438G>A	NP_001363836.1:p.Trp146Ter
NM_001376908.1:c.549G>A	NP_001363837.1:p.Trp183Ter