Canonical Allele Identifier: CA415259682

Gene: MTM1

Linked Data

• gnomAD v4: X-150660418-G-T
• MyVariant Identifiers: chrX:g.149828891G>T (hg19) ; chrX:g.150660418G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150660418G>T , CM000685.2:g.150660418G>T	GRCh38
NC_000023.10:g.149828891G>T , CM000685.1:g.149828891G>T	GRCh37
NC_000023.9:g.149579549G>T	NCBI36
NG_008199.1:g.96845G>T , LRG_839:g.96845G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*934G>T	ENSP00000509844.1:n.*934G>T
ENST00000685439.1:c.1056G>T	ENSP00000508454.1:p.Leu352Phe
ENST00000685944.1:c.1401G>T	ENSP00000509266.1:p.Leu467Phe
ENST00000686212.1:n.1003G>T
ENST00000687215.1:c.*1156G>T	ENSP00000509706.1:n.*1156G>T
ENST00000688152.1:c.*845G>T	ENSP00000509360.1:n.*845G>T
ENST00000688403.1:c.657G>T	ENSP00000508944.1:p.Leu219Phe
ENST00000689314.1:c.1446G>T	ENSP00000510607.1:p.Leu482Phe
ENST00000689694.1:c.1401G>T	ENSP00000508718.1:p.Leu467Phe
ENST00000689810.1:c.*1050G>T	ENSP00000510635.1:n.*1050G>T
ENST00000690282.1:c.657G>T	ENSP00000509809.1:p.Leu219Phe
ENST00000690351.1:c.*1053G>T	ENSP00000509728.1:n.*1053G>T
ENST00000691232.1:c.1056G>T	ENSP00000509675.1:p.Leu352Phe
ENST00000691482.1:n.2416G>T
ENST00000691686.1:c.1308G>T	ENSP00000509784.1:p.Leu436Phe
ENST00000691851.1:c.1053+10517G>T	ENSP00000510106.1:n.1053+10517G>T
ENST00000692015.1:c.1188G>T	ENSP00000510634.1:p.Leu396Phe
ENST00000692638.1:c.*1199G>T	ENSP00000509412.1:n.*1199G>T
ENST00000692852.1:c.1212G>T	ENSP00000510337.1:p.Leu404Phe
ENST00000692915.1:c.*1547G>T	ENSP00000508547.1:n.*1547G>T
ENST00000370396.7:c.1401G>T MANE Select	ENSP00000359423.3:p.Leu467Phe
ENST00000306167.11:n.1268G>T
ENST00000370396.6:c.1401G>T	ENSP00000359423.2:p.Leu467Phe
NM_000252.2:c.1401G>T , LRG_839t1:c.1401G>T	NP_000243.1:p.Leu467Phe
XM_005274687.2:c.1401G>T	XP_005274744.1:p.Leu467Phe
XM_011531170.1:c.1467G>T	XP_011529472.1:p.Leu489Phe
XM_011531171.1:c.1446G>T	XP_011529473.1:p.Leu482Phe
XM_011531172.1:c.1446G>T	XP_011529474.1:p.Leu482Phe
XM_011531173.1:c.1401G>T	XP_011529475.1:p.Leu467Phe
XM_011531173.2:c.1401G>T	XP_011529475.1:p.Leu467Phe
XM_017029547.1:c.1446G>T	XP_016885036.1:p.Leu482Phe
XM_017029548.1:c.1446G>T	XP_016885037.1:p.Leu482Phe
XM_017029549.1:c.1401G>T	XP_016885038.1:p.Leu467Phe
XM_017029550.1:c.1290G>T	XP_016885039.1:p.Leu430Phe
XM_017029551.2:c.657G>T	XP_016885040.1:p.Leu219Phe
NM_000252.3:c.1401G>T MANE Select	NP_000243.1:p.Leu467Phe
NM_001376906.1:c.1401G>T	NP_001363835.1:p.Leu467Phe
NM_001376907.1:c.1290G>T	NP_001363836.1:p.Leu430Phe
NM_001376908.1:c.1401G>T	NP_001363837.1:p.Leu467Phe