Canonical Allele Identifier: CA1931907725
Gene: PAX2 HGNC NCBI

Linked Data

dbSNP Id: rs1845403444

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100750580_100750582dup , CM000672.2:g.100750580_100750582dup GRCh38
NC_000010.10:g.102510337_102510339dup , CM000672.1:g.102510337_102510339dup GRCh37
NC_000010.9:g.102500327_102500329dup NCBI36
NG_008680.1:g.9870_9872dup
NG_008680.2:g.19872_19874dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000707078.1:c.306-114_306-112dup ENSP00000516729.1:n.306-114_306-112dup
ENST00000707079.1:c.213-114_213-112dup ENSP00000516730.1:n.213-114_213-112dup
ENST00000355243.8:c.213-114_213-112dup MANE Select ENSP00000347385.3:n.213-114_213-112dup
ENST00000427256.6:c.213-114_213-112dup ENSP00000398652.2:n.213-114_213-112dup
ENST00000679374.1:c.195-114_195-112dup ENSP00000506041.1:n.195-114_195-112dup
ENST00000355243.7:c.213-114_213-112dup ENSP00000347385.2:n.213-114_213-112dup
ENST00000361791.7:c.210-114_210-112dup ENSP00000355069.4:n.210-114_210-112dup
ENST00000370296.6:c.213-114_213-112dup ENSP00000359319.3:n.213-114_213-112dup
ENST00000427256.5:c.213-114_213-112dup ENSP00000398652.1:n.213-114_213-112dup
ENST00000428433.5:c.213-114_213-112dup ENSP00000396259.1:n.213-114_213-112dup
ENST00000553492.5:n.131+14847_131+14849dup
ENST00000554172.2:c.225-114_225-112dup ENSP00000452489.2:n.225-114_225-112dup
ENST00000554363.2:n.125+4277_125+4279dup
NM_000278.3:c.213-114_213-112dup NP_000269.2:n.213-114_213-112dup
NM_001304569.1:c.306-114_306-112dup NP_001291498.1:n.306-114_306-112dup
NM_003987.3:c.213-114_213-112dup NP_003978.2:n.213-114_213-112dup
NM_003988.3:c.213-114_213-112dup NP_003979.2:n.213-114_213-112dup
NM_003989.3:c.213-114_213-112dup NP_003980.2:n.213-114_213-112dup
NM_003990.3:c.213-114_213-112dup NP_003981.2:n.213-114_213-112dup
NM_000278.4:c.213-114_213-112dup NP_000269.3:n.213-114_213-112dup
NM_003987.4:c.213-114_213-112dup NP_003978.3:n.213-114_213-112dup
NM_003988.4:c.213-114_213-112dup NP_003979.2:n.213-114_213-112dup
NM_003989.4:c.213-114_213-112dup NP_003980.3:n.213-114_213-112dup
NM_003990.4:c.213-114_213-112dup NP_003981.3:n.213-114_213-112dup
NM_000278.5:c.213-114_213-112dup MANE Select NP_000269.3:n.213-114_213-112dup
NM_001304569.2:c.306-114_306-112dup NP_001291498.1:n.306-114_306-112dup
NM_003987.5:c.213-114_213-112dup NP_003978.3:n.213-114_213-112dup
NM_003988.5:c.213-114_213-112dup NP_003979.2:n.213-114_213-112dup
NM_003989.5:c.213-114_213-112dup NP_003980.3:n.213-114_213-112dup
NM_003990.5:c.213-114_213-112dup NP_003981.3:n.213-114_213-112dup