Canonical Allele Identifier: CA369174480

Gene: PAX4

Linked Data

• dbSNP Id: rs2116137700
• MyVariant Identifiers: chr7:g.127253867T>C (hg19) ; chr7:g.127613813T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.127613813T>C , CM000669.2:g.127613813T>C	GRCh38
NC_000007.13:g.127253867T>C , CM000669.1:g.127253867T>C	GRCh37
NC_000007.12:g.127041103T>C	NCBI36
NG_012848.1:g.6914A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000639438.3:c.505A>G MANE Select	ENSP00000491782.1:p.Thr169Ala
ENST00000338516.7:c.505A>G	ENSP00000344297.4:p.Thr169Ala
ENST00000341640.6:c.481A>G	ENSP00000339906.2:p.Thr161Ala
ENST00000378740.6:c.481A>G	ENSP00000368014.3:p.Thr161Ala
ENST00000463946.5:c.475A>G	ENSP00000451923.1:p.Thr159Ala
ENST00000477423.1:n.475A>G
ENST00000483494.5:c.475A>G	ENSP00000473846.1:p.Thr159Ala
ENST00000611453.1:c.475A>G	ENSP00000477877.1:p.Thr159Ala
NM_006193.2:c.481A>G	NP_006184.2:p.Thr161Ala
XM_011516276.1:c.505A>G	XP_011514578.1:p.Thr169Ala
NM_001366110.1:c.505A>G MANE Select	NP_001353039.1:p.Thr169Ala
NM_001366111.1:c.505A>G	NP_001353040.1:p.Thr169Ala