Canonical Allele Identifier: CA166112959

Gene: PAX4

Linked Data

• dbSNP Id: rs751901490
• MyVariant Identifiers: chr7:g.127253792T>G (hg19) ; chr7:g.127613738T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.127613738T>G , CM000669.2:g.127613738T>G	GRCh38
NC_000007.13:g.127253792T>G , CM000669.1:g.127253792T>G	GRCh37
NC_000007.12:g.127041028T>G	NCBI36
NG_012848.1:g.6989A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000639438.3:c.562+18A>C MANE Select	ENSP00000491782.1:n.562+18A>C
ENST00000338516.7:c.562+18A>C	ENSP00000344297.4:n.562+18A>C
ENST00000341640.6:c.538+18A>C	ENSP00000339906.2:n.538+18A>C
ENST00000378740.6:c.538+18A>C	ENSP00000368014.3:n.538+18A>C
ENST00000463946.5:c.532+18A>C	ENSP00000451923.1:n.532+18A>C
ENST00000477423.1:n.532+18A>C
ENST00000483494.5:c.532+18A>C	ENSP00000473846.1:n.532+18A>C
ENST00000611453.1:c.532+18A>C	ENSP00000477877.1:n.532+18A>C
NM_006193.2:c.538+18A>C	NP_006184.2:n.538+18A>C
XM_011516276.1:c.562+18A>C	XP_011514578.1:n.562+18A>C
NM_001366110.1:c.562+18A>C MANE Select	NP_001353039.1:n.562+18A>C
NM_001366111.1:c.562+18A>C	NP_001353040.1:n.562+18A>C