Canonical Allele Identifier: CA1742009982

Gene: PAX4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.127614497G= , CM000669.2:g.127614497G=	GRCh38
NC_000007.13:g.127254551G= , CM000669.1:g.127254551G=	GRCh37
NC_000007.12:g.127041787G=	NCBI36
NG_012848.1:g.6230C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001366110.1:c.421C= MANE Select	NP_001353039.1:p.Arg141=
ENST00000639438.3:c.421C= MANE Select	ENSP00000491782.1:p.Arg141=
NM_001366111.1:c.421C=	NP_001353040.1:p.Arg141=
NM_006193.2:c.397C=	NP_006184.2:p.Arg133=
ENST00000338516.7:c.421C=	ENSP00000344297.4:p.Arg141=
ENST00000341640.6:c.397C=	ENSP00000339906.2:p.Arg133=
ENST00000378740.6:c.397C=	ENSP00000368014.3:p.Arg133=
ENST00000463946.5:c.391C=	ENSP00000451923.1:p.Arg131=
ENST00000477423.1:n.391C=
ENST00000483494.5:c.391C=	ENSP00000473846.1:p.Arg131=
ENST00000611453.1:c.391C=	ENSP00000477877.1:p.Arg131=
XM_011516276.1:c.421C=	XP_011514578.1:p.Arg141=