Canonical Allele Identifier: CA1330502918

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222202327_222202329delinsACC , CM000664.2:g.222202327_222202329delinsACC	GRCh38
NC_000002.11:g.223067046_223067048delinsACC , CM000664.1:g.223067046_223067048delinsACC	GRCh37
NC_000002.10:g.222775290_222775292delinsACC	NCBI36
NG_011632.1:g.101653_101655delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.1174-887_1174-885delinsGGT	ENSP00000338767.5:n.1174-887_1174-885delinsGGT
ENST00000344493.9:c.1174-887_1174-885delinsGGT	ENSP00000342092.4:n.1174-887_1174-885delinsGGT
ENST00000350526.9:c.1174-139_1174-137delinsGGT	ENSP00000343052.4:n.1174-139_1174-137delinsGGT
ENST00000392070.7:c.1174-139_1174-137delinsGGT MANE Select	ENSP00000375922.3:n.1174-139_1174-137delinsGGT
ENST00000464706.6:n.612-139_612-137delinsGGT
ENST00000644699.1:n.500-139_500-137delinsGGT
ENST00000646154.1:n.988-139_988-137delinsGGT
ENST00000336840.10:c.1174-887_1174-885delinsGGT	ENSP00000338767.5:n.1174-887_1174-885delinsGGT
ENST00000344493.8:c.1174-887_1174-885delinsGGT	ENSP00000342092.4:n.1174-887_1174-885delinsGGT
ENST00000350526.8:c.1174-139_1174-137delinsGGT	ENSP00000343052.4:n.1174-139_1174-137delinsGGT
ENST00000392069.6:c.1174-139_1174-137delinsGGT	ENSP00000375921.2:n.1174-139_1174-137delinsGGT
ENST00000392070.6:c.1174-139_1174-137delinsGGT	ENSP00000375922.2:n.1174-139_1174-137delinsGGT
ENST00000409551.7:c.1171-139_1171-137delinsGGT	ENSP00000386750.3:n.1171-139_1171-137delinsGGT
ENST00000464706.5:n.598-139_598-137delinsGGT
ENST00000555548.1:n.405-139_405-137delinsGGT
NM_001127366.2:c.1171-139_1171-137delinsGGT	NP_001120838.1:n.1171-139_1171-137delinsGGT
NM_181457.3:c.1174-139_1174-137delinsGGT	NP_852122.1:n.1174-139_1174-137delinsGGT
NM_181458.3:c.1174-139_1174-137delinsGGT	NP_852123.1:n.1174-139_1174-137delinsGGT
NM_181459.3:c.1174-139_1174-137delinsGGT	NP_852124.1:n.1174-139_1174-137delinsGGT
NM_181460.3:c.1174-887_1174-885delinsGGT	NP_852125.1:n.1174-887_1174-885delinsGGT
NM_181461.3:c.1174-887_1174-885delinsGGT	NP_852126.1:n.1174-887_1174-885delinsGGT
XM_011511278.1:c.1318-139_1318-137delinsGGT	XP_011509580.1:n.1318-139_1318-137delinsGGT
XM_011511279.1:c.610-139_610-137delinsGGT	XP_011509581.1:n.610-139_610-137delinsGGT
NM_001127366.3:c.1171-139_1171-137delinsGGT	NP_001120838.1:n.1171-139_1171-137delinsGGT
NM_181457.4:c.1174-139_1174-137delinsGGT	NP_852122.1:n.1174-139_1174-137delinsGGT
NM_181458.4:c.1174-139_1174-137delinsGGT MANE Select	NP_852123.1:n.1174-139_1174-137delinsGGT
NM_181459.4:c.1174-139_1174-137delinsGGT	NP_852124.1:n.1174-139_1174-137delinsGGT
NM_181460.4:c.1174-887_1174-885delinsGGT	NP_852125.1:n.1174-887_1174-885delinsGGT
NM_181461.4:c.1174-887_1174-885delinsGGT	NP_852126.1:n.1174-887_1174-885delinsGGT