Canonical Allele Identifier: CA10539170

Gene: MTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150645884A>C , CM000685.2:g.150645884A>C	GRCh38
NC_000023.10:g.149814357A>C , CM000685.1:g.149814357A>C	GRCh37
NC_000023.9:g.149565015A>C	NCBI36
NG_008199.1:g.82311A>C , LRG_839:g.82311A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*400+13A>C	ENSP00000509844.1:n.*400+13A>C
ENST00000685439.1:c.522+13A>C	ENSP00000508454.1:n.522+13A>C
ENST00000685944.1:c.867+13A>C	ENSP00000509266.1:n.867+13A>C
ENST00000686212.1:n.469+13A>C
ENST00000687215.1:c.*622+13A>C	ENSP00000509706.1:n.*622+13A>C
ENST00000688152.1:c.*311+13A>C	ENSP00000509360.1:n.*311+13A>C
ENST00000688403.1:c.123+13A>C	ENSP00000508944.1:n.123+13A>C
ENST00000689314.1:c.912+13A>C	ENSP00000510607.1:n.912+13A>C
ENST00000689694.1:c.867+13A>C	ENSP00000508718.1:n.867+13A>C
ENST00000689810.1:c.*516+13A>C	ENSP00000510635.1:n.*516+13A>C
ENST00000690282.1:c.123+13A>C	ENSP00000509809.1:n.123+13A>C
ENST00000690351.1:c.*519+13A>C	ENSP00000509728.1:n.*519+13A>C
ENST00000691232.1:c.522+13A>C	ENSP00000509675.1:n.522+13A>C
ENST00000691482.1:n.1882+13A>C
ENST00000691686.1:c.867+13A>C	ENSP00000509784.1:n.867+13A>C
ENST00000691851.1:c.867+13A>C	ENSP00000510106.1:n.867+13A>C
ENST00000692015.1:c.654+13A>C	ENSP00000510634.1:n.654+13A>C
ENST00000692638.1:c.*672+13A>C	ENSP00000509412.1:n.*672+13A>C
ENST00000692852.1:c.679-3832A>C	ENSP00000510337.1:n.679-3832A>C
ENST00000692915.1:c.*1074+13A>C	ENSP00000508547.1:n.*1074+13A>C
ENST00000370396.7:c.867+13A>C MANE Select	ENSP00000359423.3:n.867+13A>C
ENST00000306167.11:n.734+13A>C
ENST00000370396.6:c.867+13A>C	ENSP00000359423.2:n.867+13A>C
NM_000252.2:c.867+13A>C , LRG_839t1:c.867+13A>C	NP_000243.1:n.867+13A>C
XM_005274687.2:c.867+13A>C	XP_005274744.1:n.867+13A>C
XM_011531170.1:c.933+13A>C	XP_011529472.1:n.933+13A>C
XM_011531171.1:c.912+13A>C	XP_011529473.1:n.912+13A>C
XM_011531172.1:c.912+13A>C	XP_011529474.1:n.912+13A>C
XM_011531173.1:c.867+13A>C	XP_011529475.1:n.867+13A>C
XM_011531173.2:c.867+13A>C	XP_011529475.1:n.867+13A>C
XM_017029547.1:c.912+13A>C	XP_016885036.1:n.912+13A>C
XM_017029548.1:c.912+13A>C	XP_016885037.1:n.912+13A>C
XM_017029549.1:c.867+13A>C	XP_016885038.1:n.867+13A>C
XM_017029550.1:c.756+13A>C	XP_016885039.1:n.756+13A>C
XM_017029551.2:c.123+13A>C	XP_016885040.1:n.123+13A>C
NM_000252.3:c.867+13A>C MANE Select	NP_000243.1:n.867+13A>C
NM_001376906.1:c.867+13A>C	NP_001363835.1:n.867+13A>C
NM_001376907.1:c.756+13A>C	NP_001363836.1:n.756+13A>C
NM_001376908.1:c.867+13A>C	NP_001363837.1:n.867+13A>C