Canonical Allele Identifier: CA415256124
Gene: MTM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641347G>C , CM000685.2:g.150641347G>C GRCh38
NC_000023.10:g.149809820G>C , CM000685.1:g.149809820G>C GRCh37
NC_000023.9:g.149560478G>C NCBI36
NG_008199.1:g.77774G>C , LRG_839:g.77774G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*140G>C ENSP00000509844.1:n.*140G>C
ENST00000685439.1:c.262G>C ENSP00000508454.1:p.Val88Leu
ENST00000685944.1:c.607G>C ENSP00000509266.1:p.Val203Leu
ENST00000686212.1:n.209G>C
ENST00000687215.1:c.*362G>C ENSP00000509706.1:n.*362G>C
ENST00000688152.1:c.*51G>C ENSP00000509360.1:n.*51G>C
ENST00000688403.1:c.-138G>C ENSP00000508944.1:n.-138G>C
ENST00000689314.1:c.652G>C ENSP00000510607.1:p.Val218Leu
ENST00000689694.1:c.607G>C ENSP00000508718.1:p.Val203Leu
ENST00000689810.1:c.*256G>C ENSP00000510635.1:n.*256G>C
ENST00000690282.1:c.-138G>C ENSP00000509809.1:n.-138G>C
ENST00000690351.1:c.*259G>C ENSP00000509728.1:n.*259G>C
ENST00000691232.1:c.262G>C ENSP00000509675.1:p.Val88Leu
ENST00000691482.1:n.1622G>C
ENST00000691686.1:c.607G>C ENSP00000509784.1:p.Val203Leu
ENST00000691851.1:c.607G>C ENSP00000510106.1:p.Val203Leu
ENST00000692015.1:c.394G>C ENSP00000510634.1:p.Val132Leu
ENST00000692638.1:c.*412G>C ENSP00000509412.1:n.*412G>C
ENST00000692852.1:c.607G>C ENSP00000510337.1:p.Val203Leu
ENST00000692915.1:c.*814G>C ENSP00000508547.1:n.*814G>C
ENST00000370396.7:c.607G>C MANE Select ENSP00000359423.3:p.Val203Leu
ENST00000306167.11:n.474G>C
ENST00000370396.6:c.607G>C ENSP00000359423.2:p.Val203Leu
ENST00000490530.1:n.546G>C
NM_000252.2:c.607G>C , LRG_839t1:c.607G>C NP_000243.1:p.Val203Leu
XM_005274687.2:c.607G>C XP_005274744.1:p.Val203Leu
XM_011531170.1:c.673G>C XP_011529472.1:p.Val225Leu
XM_011531171.1:c.652G>C XP_011529473.1:p.Val218Leu
XM_011531172.1:c.652G>C XP_011529474.1:p.Val218Leu
XM_011531173.1:c.607G>C XP_011529475.1:p.Val203Leu
XM_011531173.2:c.607G>C XP_011529475.1:p.Val203Leu
XM_017029547.1:c.652G>C XP_016885036.1:p.Val218Leu
XM_017029548.1:c.652G>C XP_016885037.1:p.Val218Leu
XM_017029549.1:c.607G>C XP_016885038.1:p.Val203Leu
XM_017029550.1:c.496G>C XP_016885039.1:p.Val166Leu
XM_017029551.2:c.-138G>C XP_016885040.1:n.-138G>C
NM_000252.3:c.607G>C MANE Select NP_000243.1:p.Val203Leu
NM_001376906.1:c.607G>C NP_001363835.1:p.Val203Leu
NM_001376907.1:c.496G>C NP_001363836.1:p.Val166Leu
NM_001376908.1:c.607G>C NP_001363837.1:p.Val203Leu