Canonical Allele Identifier: CA378258591

Gene: PAX2

Linked Data

• MyVariant Identifiers: chr10:g.102541084T>C (hg19) ; chr10:g.100781327T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100781327T>C , CM000672.2:g.100781327T>C	GRCh38
NC_000010.10:g.102541084T>C , CM000672.1:g.102541084T>C	GRCh37
NC_000010.9:g.102531074T>C	NCBI36
NG_008680.1:g.40617T>C
NG_008680.2:g.50619T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707078.1:c.671T>C	ENSP00000516729.1:p.Ile224Thr
ENST00000707079.1:c.578T>C	ENSP00000516730.1:p.Ile193Thr
ENST00000355243.8:c.578T>C MANE Select	ENSP00000347385.3:p.Ile193Thr
ENST00000427256.6:c.578T>C	ENSP00000398652.2:p.Ile193Thr
ENST00000679374.1:c.560T>C	ENSP00000506041.1:p.Ile187Thr
ENST00000355243.7:c.578T>C	ENSP00000347385.2:p.Ile193Thr
ENST00000361791.7:c.575T>C	ENSP00000355069.4:p.Ile192Thr
ENST00000370296.6:c.578T>C	ENSP00000359319.3:p.Ile193Thr
ENST00000427256.5:c.578T>C	ENSP00000398652.1:p.Ile193Thr
ENST00000428433.5:c.578T>C	ENSP00000396259.1:p.Ile193Thr
ENST00000553492.5:n.299T>C
ENST00000554172.2:c.590T>C	ENSP00000452489.2:p.Ile197Thr
ENST00000554363.2:n.293T>C
NM_000278.3:c.578T>C	NP_000269.2:p.Ile193Thr
NM_001304569.1:c.671T>C	NP_001291498.1:p.Ile224Thr
NM_003987.3:c.578T>C	NP_003978.2:p.Ile193Thr
NM_003988.3:c.578T>C	NP_003979.2:p.Ile193Thr
NM_003989.3:c.578T>C	NP_003980.2:p.Ile193Thr
NM_003990.3:c.578T>C	NP_003981.2:p.Ile193Thr
NM_000278.4:c.578T>C	NP_000269.3:p.Ile193Thr
NM_003987.4:c.578T>C	NP_003978.3:p.Ile193Thr
NM_003988.4:c.578T>C	NP_003979.2:p.Ile193Thr
NM_003989.4:c.578T>C	NP_003980.3:p.Ile193Thr
NM_003990.4:c.578T>C	NP_003981.3:p.Ile193Thr
NM_000278.5:c.578T>C MANE Select	NP_000269.3:p.Ile193Thr
NM_001304569.2:c.671T>C	NP_001291498.1:p.Ile224Thr
NM_003987.5:c.578T>C	NP_003978.3:p.Ile193Thr
NM_003988.5:c.578T>C	NP_003979.2:p.Ile193Thr
NM_003989.5:c.578T>C	NP_003980.3:p.Ile193Thr
NM_003990.5:c.578T>C	NP_003981.3:p.Ile193Thr