Canonical Allele Identifier: CA457525062
Gene: PAX4 HGNC NCBI

Linked Data

dbSNP Id: rs1794692548
MyVariant Identifiers: chr7:g.127254597G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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