Canonical Allele Identifier: CA366177418

Gene: TIAM2

Linked Data

• MyVariant Identifiers: chr6:g.155451476G>C (hg19) ; chr6:g.155130342G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155130342G>C , CM000668.2:g.155130342G>C	GRCh38
NC_000006.11:g.155451476G>C , CM000668.1:g.155451476G>C	GRCh37
NC_000006.10:g.155493168G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682666.1:c.1119G>C MANE Select	ENSP00000507157.1:p.Lys373Asn
ENST00000318981.9:c.1119G>C	ENSP00000327315.5:p.Lys373Asn
ENST00000360366.8:c.1119G>C	ENSP00000353528.4:p.Lys373Asn
ENST00000461783.7:c.1119G>C	ENSP00000437188.2:p.Lys373Asn
ENST00000528535.5:c.1119G>C	ENSP00000434901.1:p.Lys373Asn
ENST00000529824.6:c.1119G>C	ENSP00000433348.2:p.Lys373Asn
NM_012454.3:c.1119G>C	NP_036586.2:p.Lys373Asn
NM_001384546.1:c.1119G>C	NP_001371475.1:p.Lys373Asn
NM_001384547.1:c.1119G>C	NP_001371476.1:p.Lys373Asn
NM_012454.4:c.1119G>C MANE Select	NP_036586.3:p.Lys373Asn