Canonical Allele Identifier: CA8475400

Gene: TP53I13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29569345G>A , CM000679.2:g.29569345G>A	GRCh38
NC_000017.10:g.27896363G>A , CM000679.1:g.27896363G>A	GRCh37
NC_000017.9:g.24920489G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_138349.4:c.169G>A MANE Select	NP_612358.3:p.Val57Met
ENST00000301057.8:c.169G>A MANE Select	ENSP00000301057.7:p.Val57Met
NM_001346077.1:c.94G>A	NP_001333006.1:p.Val32Met
NM_001346078.1:c.94G>A	NP_001333007.1:p.Val32Met
NM_001346079.1:c.169G>A	NP_001333008.1:p.Val57Met
NM_001346079.2:c.169G>A	NP_001333008.1:p.Val57Met
NM_001346081.1:c.-76G>A	NP_001333010.1:n.-76G>A
NM_001346081.2:c.-76G>A	NP_001333010.1:n.-76G>A
NM_001346082.1:c.-205G>A	NP_001333011.1:n.-205G>A
NM_138349.2:c.169G>A	NP_612358.3:p.Val57Met
NM_138349.3:c.169G>A	NP_612358.3:p.Val57Met
ENST00000301057.7:c.169G>A	ENSP00000301057.7:p.Val57Met
ENST00000577934.5:c.129G>A
ENST00000578749.5:c.94G>A	ENSP00000468265.1:p.Val32Met
ENST00000580132.1:n.399G>A
ENST00000580183.6:c.94G>A	ENSP00000466027.1:p.Val32Met
ENST00000581411.6:c.94G>A	ENSP00000462693.2:p.Val32Met
ENST00000582829.6:c.94G>A	ENSP00000465112.1:p.Val32Met
ENST00000583940.5:c.94G>A	ENSP00000465824.1:p.Val32Met
XM_011525442.1:c.94G>A	XP_011523744.1:p.Val32Met
XM_011525443.1:c.94G>A	XP_011523745.1:p.Val32Met
XM_011525444.1:c.94G>A	XP_011523746.1:p.Val32Met
XM_011525445.1:c.94G>A	XP_011523747.1:p.Val32Met
XM_011525446.1:c.94G>A	XP_011523748.1:p.Val32Met
XM_011525447.1:c.94G>A	XP_011523749.1:p.Val32Met
XM_011525448.1:c.-131G>A	XP_011523750.1:n.-131G>A
XM_011525449.1:c.-205G>A	XP_011523751.1:n.-205G>A
XM_024451016.1:c.94G>A	XP_024306784.1:p.Val32Met
XM_024451017.1:c.94G>A	XP_024306785.1:p.Val32Met
XM_024451018.1:c.-205G>A	XP_024306786.1:n.-205G>A