Canonical Allele Identifier: CA10539679

Gene: MTMR1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150762633C>T , CM000685.2:g.150762633C>T	GRCh38
NC_000023.10:g.149931106C>T , CM000685.1:g.149931106C>T	GRCh37
NC_000023.9:g.149681764C>T	NCBI36
NG_012551.1:g.74238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490316.7:c.1953C>T	ENSP00000436957.2:p.Gly651=
ENST00000445323.7:c.1926C>T MANE Select	ENSP00000414178.2:p.Gly642=
ENST00000370390.7:c.1902C>T	ENSP00000359417.3:p.Gly634=
ENST00000445323.6:c.1926C>T	ENSP00000414178.2:p.Gly642=
ENST00000485376.5:c.*406C>T	ENSP00000434105.1:n.*406C>T
ENST00000488357.1:c.1555-1879C>T
NM_001306144.1:c.1926C>T	NP_001293073.1:p.Gly642=
NM_003828.2:c.1902C>T	NP_003819.1:p.Gly634=
NM_003828.3:c.1902C>T	NP_003819.1:p.Gly634=
XM_005274765.2:c.2004C>T	XP_005274822.1:p.Gly668=
XM_005274766.2:c.1953C>T	XP_005274823.1:p.Gly651=
XM_005274767.2:c.1953C>T	XP_005274824.1:p.Gly651=
XM_006724854.2:c.1977C>T	XP_006724917.1:p.Gly659=
XM_006724855.2:c.1902C>T	XP_006724918.1:p.Gly634=
XM_006724856.2:c.1620C>T	XP_006724919.1:p.Gly540=
XM_011531208.1:c.1827C>T	XP_011529510.1:p.Gly609=
XM_011531209.1:c.1620C>T	XP_011529511.1:p.Gly540=
NM_001306144.2:c.1926C>T	NP_001293073.1:p.Gly642=
NM_001353990.1:c.1953C>T	NP_001340919.1:p.Gly651=
NM_001353991.1:c.1620C>T	NP_001340920.1:p.Gly540=
NM_001353992.1:c.1620C>T	NP_001340921.1:p.Gly540=
NM_001353993.1:c.1620C>T	NP_001340922.1:p.Gly540=
NM_001353994.1:c.1620C>T	NP_001340923.1:p.Gly540=
NM_001353995.1:c.1620C>T	NP_001340924.1:p.Gly540=
NM_001353996.1:c.1620C>T	NP_001340925.1:p.Gly540=
NR_148676.1:n.2280C>T
XM_005274765.3:c.2004C>T	XP_005274822.1:p.Gly668=
XM_005274766.3:c.1953C>T	XP_005274823.1:p.Gly651=
XM_006724855.3:c.1902C>T	XP_006724918.1:p.Gly634=
XM_017029921.1:c.1620C>T	XP_016885410.1:p.Gly540=
XM_017029923.1:c.1563C>T	XP_016885412.1:p.Gly521=
XR_001755740.1:n.2280C>T
NM_001306144.3:c.1926C>T MANE Select	NP_001293073.1:p.Gly642=
NM_001353990.2:c.1953C>T	NP_001340919.1:p.Gly651=
NM_003828.4:c.1902C>T	NP_003819.1:p.Gly634=
NR_148676.2:n.2248C>T
NM_003828.5:c.1902C>T	NP_003819.1:p.Gly634=
NR_148676.3:n.2248C>T