Canonical Allele Identifier: CA519113264

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149809813T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641340T>C , CM000685.2:g.150641340T>C	GRCh38
NC_000023.10:g.149809813T>C , CM000685.1:g.149809813T>C	GRCh37
NC_000023.9:g.149560471T>C	NCBI36
NG_008199.1:g.77767T>C , LRG_839:g.77767T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*133T>C	ENSP00000509844.1:n.*133T>C
ENST00000685439.1:c.255T>C	ENSP00000508454.1:p.Ala85=
ENST00000685944.1:c.600T>C	ENSP00000509266.1:p.Ala200=
ENST00000686212.1:n.202T>C
ENST00000687215.1:c.*355T>C	ENSP00000509706.1:n.*355T>C
ENST00000688152.1:c.*44T>C	ENSP00000509360.1:n.*44T>C
ENST00000688403.1:c.-145T>C	ENSP00000508944.1:n.-145T>C
ENST00000689314.1:c.645T>C	ENSP00000510607.1:p.Ala215=
ENST00000689694.1:c.600T>C	ENSP00000508718.1:p.Ala200=
ENST00000689810.1:c.*249T>C	ENSP00000510635.1:n.*249T>C
ENST00000690282.1:c.-145T>C	ENSP00000509809.1:n.-145T>C
ENST00000690351.1:c.*252T>C	ENSP00000509728.1:n.*252T>C
ENST00000691232.1:c.255T>C	ENSP00000509675.1:p.Ala85=
ENST00000691482.1:n.1615T>C
ENST00000691686.1:c.600T>C	ENSP00000509784.1:p.Ala200=
ENST00000691851.1:c.600T>C	ENSP00000510106.1:p.Ala200=
ENST00000692015.1:c.387T>C	ENSP00000510634.1:p.Ala129=
ENST00000692638.1:c.*405T>C	ENSP00000509412.1:n.*405T>C
ENST00000692852.1:c.600T>C	ENSP00000510337.1:p.Ala200=
ENST00000692915.1:c.*807T>C	ENSP00000508547.1:n.*807T>C
ENST00000370396.7:c.600T>C MANE Select	ENSP00000359423.3:p.Ala200=
ENST00000306167.11:n.467T>C
ENST00000370396.6:c.600T>C	ENSP00000359423.2:p.Ala200=
ENST00000490530.1:n.539T>C
NM_000252.2:c.600T>C , LRG_839t1:c.600T>C	NP_000243.1:p.Ala200=
XM_005274687.2:c.600T>C	XP_005274744.1:p.Ala200=
XM_011531170.1:c.666T>C	XP_011529472.1:p.Ala222=
XM_011531171.1:c.645T>C	XP_011529473.1:p.Ala215=
XM_011531172.1:c.645T>C	XP_011529474.1:p.Ala215=
XM_011531173.1:c.600T>C	XP_011529475.1:p.Ala200=
XM_011531173.2:c.600T>C	XP_011529475.1:p.Ala200=
XM_017029547.1:c.645T>C	XP_016885036.1:p.Ala215=
XM_017029548.1:c.645T>C	XP_016885037.1:p.Ala215=
XM_017029549.1:c.600T>C	XP_016885038.1:p.Ala200=
XM_017029550.1:c.489T>C	XP_016885039.1:p.Ala163=
XM_017029551.2:c.-145T>C	XP_016885040.1:n.-145T>C
NM_000252.3:c.600T>C MANE Select	NP_000243.1:p.Ala200=
NM_001376906.1:c.600T>C	NP_001363835.1:p.Ala200=
NM_001376907.1:c.489T>C	NP_001363836.1:p.Ala163=
NM_001376908.1:c.600T>C	NP_001363837.1:p.Ala200=