Canonical Allele Identifier: CA9998504

Gene: TIAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31252009C>G , CM000683.2:g.31252009C>G	GRCh38
NC_000021.8:g.32624325C>G , CM000683.1:g.32624325C>G	GRCh37
NC_000021.7:g.31546196C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001353694.2:c.1144G>C MANE Select	NP_001340623.1:p.Gly382Arg
ENST00000541036.6:c.1144G>C MANE Select	ENSP00000441570.2:p.Gly382Arg
NM_001353686.1:c.1144G>C	NP_001340615.1:p.Gly382Arg
NM_001353686.2:c.1144G>C	NP_001340615.1:p.Gly382Arg
NM_001353687.1:c.1144G>C	NP_001340616.1:p.Gly382Arg
NM_001353687.2:c.1144G>C	NP_001340616.1:p.Gly382Arg
NM_001353688.1:c.1144G>C	NP_001340617.1:p.Gly382Arg
NM_001353689.1:c.1144G>C	NP_001340618.1:p.Gly382Arg
NM_001353690.1:c.1144G>C	NP_001340619.1:p.Gly382Arg
NM_001353691.1:c.1144G>C	NP_001340620.1:p.Gly382Arg
NM_001353692.1:c.1144G>C	NP_001340621.1:p.Gly382Arg
NM_001353693.1:c.1144G>C	NP_001340622.1:p.Gly382Arg
NM_001353694.1:c.1144G>C	NP_001340623.1:p.Gly382Arg
NM_003253.2:c.1144G>C	NP_003244.2:p.Gly382Arg
NM_003253.3:c.1144G>C	NP_003244.2:p.Gly382Arg
ENST00000286827.7:c.1144G>C	ENSP00000286827.3:p.Gly382Arg
ENST00000455508.2:c.1144G>C	ENSP00000388217.2:p.Gly382Arg
ENST00000469412.5:n.473G>C
ENST00000541036.5:c.1144G>C	ENSP00000441570.1:p.Gly382Arg
ENST00000698169.1:c.1144G>C	ENSP00000513591.1:p.Gly382Arg
XM_005261037.1:c.1144G>C	XP_005261094.1:p.Gly382Arg
XM_005261038.1:c.1144G>C	XP_005261095.1:p.Gly382Arg
XM_005261038.3:c.1144G>C	XP_005261095.1:p.Gly382Arg
XM_005261040.1:c.1144G>C	XP_005261097.1:p.Gly382Arg
XM_005261040.2:c.1144G>C	XP_005261097.1:p.Gly382Arg
XM_011529711.1:c.1144G>C	XP_011528013.1:p.Gly382Arg
XM_011529712.1:c.1144G>C	XP_011528014.1:p.Gly382Arg
XM_011529713.1:c.1144G>C	XP_011528015.1:p.Gly382Arg
XM_017028448.1:c.1144G>C	XP_016883937.1:p.Gly382Arg
XM_017028450.1:c.1144G>C	XP_016883939.1:p.Gly382Arg
XM_017028451.2:c.1144G>C	XP_016883940.1:p.Gly382Arg
XM_024452127.1:c.1144G>C	XP_024307895.1:p.Gly382Arg