Canonical Allele Identifier: CA1931920610

Gene: PAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100806463C= , CM000672.2:g.100806463C=	GRCh38
NC_000010.10:g.102566220C= , CM000672.1:g.102566220C=	GRCh37
NC_000010.9:g.102556210C=	NCBI36
NG_008680.1:g.65753C=
NG_008680.2:g.75755C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707078.1:c.743C=	ENSP00000516729.1:p.Ser248=
ENST00000707079.1:c.719C=	ENSP00000516730.1:p.Ser240=
ENST00000355243.8:c.650C= MANE Select	ENSP00000347385.3:p.Ser217=
ENST00000427256.6:c.650C=	ENSP00000398652.2:p.Ser217=
ENST00000679374.1:c.632C=	ENSP00000506041.1:p.Ser211=
ENST00000355243.7:c.650C=	ENSP00000347385.2:p.Ser217=
ENST00000361791.7:c.647C=	ENSP00000355069.4:p.Ser216=
ENST00000370296.6:c.650C=	ENSP00000359319.3:p.Ser217=
ENST00000428433.5:c.719C=	ENSP00000396259.1:p.Ser240=
ENST00000553492.5:n.371C=
ENST00000554172.2:c.638C=	ENSP00000452489.2:p.Ser213=
ENST00000554363.2:n.365C=
NM_000278.3:c.650C=	NP_000269.2:p.Ser217=
NM_001304569.1:c.743C=	NP_001291498.1:p.Ser248=
NM_003987.3:c.719C=	NP_003978.2:p.Ser240=
NM_003988.3:c.650C=	NP_003979.2:p.Ser217=
NM_003989.3:c.650C=	NP_003980.2:p.Ser217=
NM_003990.3:c.719C=	NP_003981.2:p.Ser240=
NM_000278.4:c.650C=	NP_000269.3:p.Ser217=
NM_003987.4:c.719C=	NP_003978.3:p.Ser240=
NM_003988.4:c.650C=	NP_003979.2:p.Ser217=
NM_003989.4:c.650C=	NP_003980.3:p.Ser217=
NM_003990.4:c.719C=	NP_003981.3:p.Ser240=
NM_000278.5:c.650C= MANE Select	NP_000269.3:p.Ser217=
NM_001304569.2:c.743C=	NP_001291498.1:p.Ser248=
NM_003987.5:c.719C=	NP_003978.3:p.Ser240=
NM_003988.5:c.650C=	NP_003979.2:p.Ser217=
NM_003989.5:c.650C=	NP_003980.3:p.Ser217=
NM_003990.5:c.719C=	NP_003981.3:p.Ser240=