Canonical Allele Identifier: CA519113273

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149809825T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641352T>C , CM000685.2:g.150641352T>C	GRCh38
NC_000023.10:g.149809825T>C , CM000685.1:g.149809825T>C	GRCh37
NC_000023.9:g.149560483T>C	NCBI36
NG_008199.1:g.77779T>C , LRG_839:g.77779T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*145T>C	ENSP00000509844.1:n.*145T>C
ENST00000685439.1:c.267T>C	ENSP00000508454.1:p.Val89=
ENST00000685944.1:c.612T>C	ENSP00000509266.1:p.Val204=
ENST00000686212.1:n.214T>C
ENST00000687215.1:c.*367T>C	ENSP00000509706.1:n.*367T>C
ENST00000688152.1:c.*56T>C	ENSP00000509360.1:n.*56T>C
ENST00000688403.1:c.-133T>C	ENSP00000508944.1:n.-133T>C
ENST00000689314.1:c.657T>C	ENSP00000510607.1:p.Val219=
ENST00000689694.1:c.612T>C	ENSP00000508718.1:p.Val204=
ENST00000689810.1:c.*261T>C	ENSP00000510635.1:n.*261T>C
ENST00000690282.1:c.-133T>C	ENSP00000509809.1:n.-133T>C
ENST00000690351.1:c.*264T>C	ENSP00000509728.1:n.*264T>C
ENST00000691232.1:c.267T>C	ENSP00000509675.1:p.Val89=
ENST00000691482.1:n.1627T>C
ENST00000691686.1:c.612T>C	ENSP00000509784.1:p.Val204=
ENST00000691851.1:c.612T>C	ENSP00000510106.1:p.Val204=
ENST00000692015.1:c.399T>C	ENSP00000510634.1:p.Val133=
ENST00000692638.1:c.*417T>C	ENSP00000509412.1:n.*417T>C
ENST00000692852.1:c.612T>C	ENSP00000510337.1:p.Val204=
ENST00000692915.1:c.*819T>C	ENSP00000508547.1:n.*819T>C
ENST00000370396.7:c.612T>C MANE Select	ENSP00000359423.3:p.Val204=
ENST00000306167.11:n.479T>C
ENST00000370396.6:c.612T>C	ENSP00000359423.2:p.Val204=
ENST00000490530.1:n.551T>C
NM_000252.2:c.612T>C , LRG_839t1:c.612T>C	NP_000243.1:p.Val204=
XM_005274687.2:c.612T>C	XP_005274744.1:p.Val204=
XM_011531170.1:c.678T>C	XP_011529472.1:p.Val226=
XM_011531171.1:c.657T>C	XP_011529473.1:p.Val219=
XM_011531172.1:c.657T>C	XP_011529474.1:p.Val219=
XM_011531173.1:c.612T>C	XP_011529475.1:p.Val204=
XM_011531173.2:c.612T>C	XP_011529475.1:p.Val204=
XM_017029547.1:c.657T>C	XP_016885036.1:p.Val219=
XM_017029548.1:c.657T>C	XP_016885037.1:p.Val219=
XM_017029549.1:c.612T>C	XP_016885038.1:p.Val204=
XM_017029550.1:c.501T>C	XP_016885039.1:p.Val167=
XM_017029551.2:c.-133T>C	XP_016885040.1:n.-133T>C
NM_000252.3:c.612T>C MANE Select	NP_000243.1:p.Val204=
NM_001376906.1:c.612T>C	NP_001363835.1:p.Val204=
NM_001376907.1:c.501T>C	NP_001363836.1:p.Val167=
NM_001376908.1:c.612T>C	NP_001363837.1:p.Val204=