Canonical Allele Identifier: CA415259659

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149828881T>C (hg19) ; chrX:g.150660408T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150660408T>C , CM000685.2:g.150660408T>C	GRCh38
NC_000023.10:g.149828881T>C , CM000685.1:g.149828881T>C	GRCh37
NC_000023.9:g.149579539T>C	NCBI36
NG_008199.1:g.96835T>C , LRG_839:g.96835T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*924T>C	ENSP00000509844.1:n.*924T>C
ENST00000685439.1:c.1046T>C	ENSP00000508454.1:p.Ile349Thr
ENST00000685944.1:c.1391T>C	ENSP00000509266.1:p.Ile464Thr
ENST00000686212.1:n.993T>C
ENST00000687215.1:c.*1146T>C	ENSP00000509706.1:n.*1146T>C
ENST00000688152.1:c.*835T>C	ENSP00000509360.1:n.*835T>C
ENST00000688403.1:c.647T>C	ENSP00000508944.1:p.Ile216Thr
ENST00000689314.1:c.1436T>C	ENSP00000510607.1:p.Ile479Thr
ENST00000689694.1:c.1391T>C	ENSP00000508718.1:p.Ile464Thr
ENST00000689810.1:c.*1040T>C	ENSP00000510635.1:n.*1040T>C
ENST00000690282.1:c.647T>C	ENSP00000509809.1:p.Ile216Thr
ENST00000690351.1:c.*1043T>C	ENSP00000509728.1:n.*1043T>C
ENST00000691232.1:c.1046T>C	ENSP00000509675.1:p.Ile349Thr
ENST00000691482.1:n.2406T>C
ENST00000691686.1:c.1298T>C	ENSP00000509784.1:p.Ile433Thr
ENST00000691851.1:c.1053+10507T>C	ENSP00000510106.1:n.1053+10507T>C
ENST00000692015.1:c.1178T>C	ENSP00000510634.1:p.Ile393Thr
ENST00000692638.1:c.*1189T>C	ENSP00000509412.1:n.*1189T>C
ENST00000692852.1:c.1202T>C	ENSP00000510337.1:p.Ile401Thr
ENST00000692915.1:c.*1537T>C	ENSP00000508547.1:n.*1537T>C
ENST00000370396.7:c.1391T>C MANE Select	ENSP00000359423.3:p.Ile464Thr
ENST00000306167.11:n.1258T>C
ENST00000370396.6:c.1391T>C	ENSP00000359423.2:p.Ile464Thr
NM_000252.2:c.1391T>C , LRG_839t1:c.1391T>C	NP_000243.1:p.Ile464Thr
XM_005274687.2:c.1391T>C	XP_005274744.1:p.Ile464Thr
XM_011531170.1:c.1457T>C	XP_011529472.1:p.Ile486Thr
XM_011531171.1:c.1436T>C	XP_011529473.1:p.Ile479Thr
XM_011531172.1:c.1436T>C	XP_011529474.1:p.Ile479Thr
XM_011531173.1:c.1391T>C	XP_011529475.1:p.Ile464Thr
XM_011531173.2:c.1391T>C	XP_011529475.1:p.Ile464Thr
XM_017029547.1:c.1436T>C	XP_016885036.1:p.Ile479Thr
XM_017029548.1:c.1436T>C	XP_016885037.1:p.Ile479Thr
XM_017029549.1:c.1391T>C	XP_016885038.1:p.Ile464Thr
XM_017029550.1:c.1280T>C	XP_016885039.1:p.Ile427Thr
XM_017029551.2:c.647T>C	XP_016885040.1:p.Ile216Thr
NM_000252.3:c.1391T>C MANE Select	NP_000243.1:p.Ile464Thr
NM_001376906.1:c.1391T>C	NP_001363835.1:p.Ile464Thr
NM_001376907.1:c.1280T>C	NP_001363836.1:p.Ile427Thr
NM_001376908.1:c.1391T>C	NP_001363837.1:p.Ile464Thr