Canonical Allele Identifier: CA233175

Gene: PAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100809115C>T , CM000672.2:g.100809115C>T	GRCh38
NC_000010.10:g.102568872C>T , CM000672.1:g.102568872C>T	GRCh37
NC_000010.9:g.102558862C>T	NCBI36
NG_008680.1:g.68405C>T
NG_008680.2:g.78407C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707078.1:c.891C>T	ENSP00000516729.1:p.Asn297=
ENST00000707079.1:c.867C>T	ENSP00000516730.1:p.Asn289=
ENST00000355243.8:c.798C>T MANE Select	ENSP00000347385.3:p.Asn266=
ENST00000427256.6:c.798C>T	ENSP00000398652.2:p.Asn266=
ENST00000679374.1:c.780C>T	ENSP00000506041.1:p.Asn260=
ENST00000355243.7:c.798C>T	ENSP00000347385.2:p.Asn266=
ENST00000361791.7:c.795C>T	ENSP00000355069.4:p.Asn265=
ENST00000370296.6:c.798C>T	ENSP00000359319.3:p.Asn266=
ENST00000428433.5:c.867C>T	ENSP00000396259.1:p.Asn289=
ENST00000554172.2:c.786C>T	ENSP00000452489.2:p.Asn262=
ENST00000554363.2:n.513C>T
NM_000278.3:c.798C>T	NP_000269.2:p.Asn266=
NM_001304569.1:c.891C>T	NP_001291498.1:p.Asn297=
NM_003987.3:c.867C>T	NP_003978.2:p.Asn289=
NM_003988.3:c.798C>T	NP_003979.2:p.Asn266=
NM_003989.3:c.798C>T	NP_003980.2:p.Asn266=
NM_003990.3:c.867C>T	NP_003981.2:p.Asn289=
NM_000278.4:c.798C>T	NP_000269.3:p.Asn266=
NM_003987.4:c.867C>T	NP_003978.3:p.Asn289=
NM_003988.4:c.798C>T	NP_003979.2:p.Asn266=
NM_003989.4:c.798C>T	NP_003980.3:p.Asn266=
NM_003990.4:c.867C>T	NP_003981.3:p.Asn289=
NM_000278.5:c.798C>T MANE Select	NP_000269.3:p.Asn266=
NM_001304569.2:c.891C>T	NP_001291498.1:p.Asn297=
NM_003987.5:c.867C>T	NP_003978.3:p.Asn289=
NM_003988.5:c.798C>T	NP_003979.2:p.Asn266=
NM_003989.5:c.798C>T	NP_003980.3:p.Asn266=
NM_003990.5:c.867C>T	NP_003981.3:p.Asn289=