Canonical Allele Identifier: CA1742010030
Gene: PAX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.127614533G= , CM000669.2:g.127614533G= GRCh38
NC_000007.13:g.127254587G= , CM000669.1:g.127254587G= GRCh37
NC_000007.12:g.127041823G= NCBI36
NG_012848.1:g.6194C=

Transcript Alleles

HGVS Amino-acid Change
NM_001366110.1:c.385C= MANE Select NP_001353039.1:p.Arg129=
ENST00000639438.3:c.385C= MANE Select ENSP00000491782.1:p.Arg129=
NM_001366111.1:c.385C= NP_001353040.1:p.Arg129=
NM_006193.2:c.361C= NP_006184.2:p.Arg121=
ENST00000338516.7:c.385C= ENSP00000344297.4:p.Arg129=
ENST00000341640.6:c.361C= ENSP00000339906.2:p.Arg121=
ENST00000378740.6:c.361C= ENSP00000368014.3:p.Arg121=
ENST00000463946.5:c.355C= ENSP00000451923.1:p.Arg119=
ENST00000477423.1:n.355C=
ENST00000483494.5:c.355C= ENSP00000473846.1:p.Arg119=
ENST00000611453.1:c.355C= ENSP00000477877.1:p.Arg119=
XM_011516276.1:c.385C= XP_011514578.1:p.Arg129=