Canonical Allele Identifier: CA271782

Gene: MTM1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150659740G>A , CM000685.2:g.150659740G>A	GRCh38
NC_000023.10:g.149828213G>A , CM000685.1:g.149828213G>A	GRCh37
NC_000023.9:g.149578871G>A	NCBI36
NG_008199.1:g.96167G>A , LRG_839:g.96167G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*870G>A	ENSP00000509844.1:n.*870G>A
ENST00000685439.1:c.992G>A	ENSP00000508454.1:p.Trp331Ter
ENST00000685944.1:c.1337G>A	ENSP00000509266.1:p.Trp446Ter
ENST00000686212.1:n.939G>A
ENST00000687215.1:c.*1092G>A	ENSP00000509706.1:n.*1092G>A
ENST00000688152.1:c.*781G>A	ENSP00000509360.1:n.*781G>A
ENST00000688403.1:c.593G>A	ENSP00000508944.1:p.Trp198Ter
ENST00000689314.1:c.1382G>A	ENSP00000510607.1:p.Trp461Ter
ENST00000689694.1:c.1337G>A	ENSP00000508718.1:p.Trp446Ter
ENST00000689810.1:c.*986G>A	ENSP00000510635.1:n.*986G>A
ENST00000690282.1:c.593G>A	ENSP00000509809.1:p.Trp198Ter
ENST00000690351.1:c.*989G>A	ENSP00000509728.1:n.*989G>A
ENST00000691232.1:c.992G>A	ENSP00000509675.1:p.Trp331Ter
ENST00000691482.1:n.2352G>A
ENST00000691686.1:c.1261-631G>A	ENSP00000509784.1:n.1261-631G>A
ENST00000691851.1:c.1053+9839G>A	ENSP00000510106.1:n.1053+9839G>A
ENST00000692015.1:c.1124G>A	ENSP00000510634.1:p.Trp375Ter
ENST00000692638.1:c.*1135G>A	ENSP00000509412.1:n.*1135G>A
ENST00000692852.1:c.1148G>A	ENSP00000510337.1:p.Trp383Ter
ENST00000692915.1:c.*1483G>A	ENSP00000508547.1:n.*1483G>A
ENST00000370396.7:c.1337G>A MANE Select	ENSP00000359423.3:p.Trp446Ter
ENST00000306167.11:n.1204G>A
ENST00000370396.6:c.1337G>A	ENSP00000359423.2:p.Trp446Ter
NM_000252.2:c.1337G>A , LRG_839t1:c.1337G>A	NP_000243.1:p.Trp446Ter
XM_005274687.2:c.1337G>A	XP_005274744.1:p.Trp446Ter
XM_011531170.1:c.1403G>A	XP_011529472.1:p.Trp468Ter
XM_011531171.1:c.1382G>A	XP_011529473.1:p.Trp461Ter
XM_011531172.1:c.1382G>A	XP_011529474.1:p.Trp461Ter
XM_011531173.1:c.1337G>A	XP_011529475.1:p.Trp446Ter
XM_011531173.2:c.1337G>A	XP_011529475.1:p.Trp446Ter
XM_017029547.1:c.1382G>A	XP_016885036.1:p.Trp461Ter
XM_017029548.1:c.1382G>A	XP_016885037.1:p.Trp461Ter
XM_017029549.1:c.1337G>A	XP_016885038.1:p.Trp446Ter
XM_017029550.1:c.1226G>A	XP_016885039.1:p.Trp409Ter
XM_017029551.2:c.593G>A	XP_016885040.1:p.Trp198Ter
NM_000252.3:c.1337G>A MANE Select	NP_000243.1:p.Trp446Ter
NM_001376906.1:c.1337G>A	NP_001363835.1:p.Trp446Ter
NM_001376907.1:c.1226G>A	NP_001363836.1:p.Trp409Ter
NM_001376908.1:c.1337G>A	NP_001363837.1:p.Trp446Ter