Canonical Allele Identifier: CA1742010055
Gene: PAX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.127614543G= , CM000669.2:g.127614543G= GRCh38
NC_000007.13:g.127254597G= , CM000669.1:g.127254597G= GRCh37
NC_000007.12:g.127041833G= NCBI36
NG_012848.1:g.6184C=

Transcript Alleles

HGVS Amino-acid change
ENST00000639438.3:c.375C= MANE Select ENSP00000491782.1:p.Asn125=
ENST00000338516.7:c.375C= ENSP00000344297.4:p.Asn125=
ENST00000341640.6:c.351C= ENSP00000339906.2:p.Asn117=
ENST00000378740.6:c.351C= ENSP00000368014.3:p.Asn117=
ENST00000463946.5:c.345C= ENSP00000451923.1:p.Asn115=
ENST00000477423.1:n.345C=
ENST00000483494.5:c.345C= ENSP00000473846.1:p.Asn115=
ENST00000611453.1:c.345C= ENSP00000477877.1:p.Asn115=
NM_006193.2:c.351C= NP_006184.2:p.Asn117=
XM_011516276.1:c.375C= XP_011514578.1:p.Asn125=
NM_001366110.1:c.375C= MANE Select NP_001353039.1:p.Asn125=
NM_001366111.1:c.375C= NP_001353040.1:p.Asn125=