Canonical Allele Identifier: CA1742011095
Community Standard Title: NM_001366110.1(PAX4):c.133C= (p.Arg45=)
Gene: PAX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.127615412G= , CM000669.2:g.127615412G= GRCh38
NC_000007.13:g.127255466G= , CM000669.1:g.127255466G= GRCh37
NC_000007.12:g.127042702G= NCBI36
NG_012848.1:g.5315C=

Transcript Alleles

HGVS Amino-acid Change
NM_001366110.1:c.133C= MANE Select NP_001353039.1:p.Arg45=
ENST00000639438.3:c.133C= MANE Select ENSP00000491782.1:p.Arg45=
NM_001366111.1:c.133C= NP_001353040.1:p.Arg45=
NM_006193.2:c.109C= NP_006184.2:p.Arg37=
ENST00000338516.7:c.133C= ENSP00000344297.4:p.Arg45=
ENST00000341640.6:c.109C= ENSP00000339906.2:p.Arg37=
ENST00000378740.6:c.109C= ENSP00000368014.3:p.Arg37=
ENST00000463946.5:c.-203C= ENSP00000451923.1:n.-203C=
ENST00000483494.5:c.-203C= ENSP00000473846.1:n.-203C=
ENST00000611453.1:c.-203C= ENSP00000477877.1:n.-203C=
XM_011516276.1:c.133C= XP_011514578.1:p.Arg45=