Canonical Allele Identifier: CA4063849

Gene: TIAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155129320C>T , CM000668.2:g.155129320C>T	GRCh38
NC_000006.11:g.155450454C>T , CM000668.1:g.155450454C>T	GRCh37
NC_000006.10:g.155492146C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012454.4:c.97C>T MANE Select	NP_036586.3:p.Arg33Cys
ENST00000682666.1:c.97C>T MANE Select	ENSP00000507157.1:p.Arg33Cys
NM_001384546.1:c.97C>T	NP_001371475.1:p.Arg33Cys
NM_001384547.1:c.97C>T	NP_001371476.1:p.Arg33Cys
NM_012454.3:c.97C>T	NP_036586.2:p.Arg33Cys
ENST00000318981.9:c.97C>T	ENSP00000327315.5:p.Arg33Cys
ENST00000360366.8:c.97C>T	ENSP00000353528.4:p.Arg33Cys
ENST00000461783.7:c.97C>T	ENSP00000437188.2:p.Arg33Cys
ENST00000528535.5:c.97C>T	ENSP00000434901.1:p.Arg33Cys
ENST00000529824.6:c.97C>T	ENSP00000433348.2:p.Arg33Cys
ENST00000535231.5:c.97C>T	ENSP00000443546.1:p.Arg33Cys
ENST00000535583.1:c.97C>T	ENSP00000442989.1:p.Arg33Cys
ENST00000538270.5:c.97C>T	ENSP00000437435.1:p.Arg33Cys
ENST00000545347.5:c.97C>T	ENSP00000444040.1:p.Arg33Cys