Canonical Allele Identifier: CA415256036

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149809782A>C (hg19) ; chrX:g.150641309A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641309A>C , CM000685.2:g.150641309A>C	GRCh38
NC_000023.10:g.149809782A>C , CM000685.1:g.149809782A>C	GRCh37
NC_000023.9:g.149560440A>C	NCBI36
NG_008199.1:g.77736A>C , LRG_839:g.77736A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*102A>C	ENSP00000509844.1:n.*102A>C
ENST00000685439.1:c.224A>C	ENSP00000508454.1:p.Lys75Thr
ENST00000685944.1:c.569A>C	ENSP00000509266.1:p.Lys190Thr
ENST00000686212.1:n.171A>C
ENST00000687215.1:c.*324A>C	ENSP00000509706.1:n.*324A>C
ENST00000688152.1:c.*13A>C	ENSP00000509360.1:n.*13A>C
ENST00000688403.1:c.-176A>C	ENSP00000508944.1:n.-176A>C
ENST00000689314.1:c.614A>C	ENSP00000510607.1:p.Lys205Thr
ENST00000689694.1:c.569A>C	ENSP00000508718.1:p.Lys190Thr
ENST00000689810.1:c.*218A>C	ENSP00000510635.1:n.*218A>C
ENST00000690282.1:c.-176A>C	ENSP00000509809.1:n.-176A>C
ENST00000690351.1:c.*221A>C	ENSP00000509728.1:n.*221A>C
ENST00000691232.1:c.224A>C	ENSP00000509675.1:p.Lys75Thr
ENST00000691482.1:n.1584A>C
ENST00000691686.1:c.569A>C	ENSP00000509784.1:p.Lys190Thr
ENST00000691851.1:c.569A>C	ENSP00000510106.1:p.Lys190Thr
ENST00000692015.1:c.356A>C	ENSP00000510634.1:p.Lys119Thr
ENST00000692638.1:c.*374A>C	ENSP00000509412.1:n.*374A>C
ENST00000692852.1:c.569A>C	ENSP00000510337.1:p.Lys190Thr
ENST00000692915.1:c.*776A>C	ENSP00000508547.1:n.*776A>C
ENST00000370396.7:c.569A>C MANE Select	ENSP00000359423.3:p.Lys190Thr
ENST00000306167.11:n.436A>C
ENST00000370396.6:c.569A>C	ENSP00000359423.2:p.Lys190Thr
ENST00000490530.1:n.508A>C
NM_000252.2:c.569A>C , LRG_839t1:c.569A>C	NP_000243.1:p.Lys190Thr
XM_005274687.2:c.569A>C	XP_005274744.1:p.Lys190Thr
XM_011531170.1:c.635A>C	XP_011529472.1:p.Lys212Thr
XM_011531171.1:c.614A>C	XP_011529473.1:p.Lys205Thr
XM_011531172.1:c.614A>C	XP_011529474.1:p.Lys205Thr
XM_011531173.1:c.569A>C	XP_011529475.1:p.Lys190Thr
XM_011531173.2:c.569A>C	XP_011529475.1:p.Lys190Thr
XM_017029547.1:c.614A>C	XP_016885036.1:p.Lys205Thr
XM_017029548.1:c.614A>C	XP_016885037.1:p.Lys205Thr
XM_017029549.1:c.569A>C	XP_016885038.1:p.Lys190Thr
XM_017029550.1:c.458A>C	XP_016885039.1:p.Lys153Thr
XM_017029551.2:c.-176A>C	XP_016885040.1:n.-176A>C
NM_000252.3:c.569A>C MANE Select	NP_000243.1:p.Lys190Thr
NM_001376906.1:c.569A>C	NP_001363835.1:p.Lys190Thr
NM_001376907.1:c.458A>C	NP_001363836.1:p.Lys153Thr
NM_001376908.1:c.569A>C	NP_001363837.1:p.Lys190Thr