Canonical Allele Identifier: CA369174472

Gene: PAX4

Linked Data

• gnomAD v4: 7-127613812-G-A
• MyVariant Identifiers: chr7:g.127253866G>A (hg19) ; chr7:g.127613812G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.127613812G>A , CM000669.2:g.127613812G>A	GRCh38
NC_000007.13:g.127253866G>A , CM000669.1:g.127253866G>A	GRCh37
NC_000007.12:g.127041102G>A	NCBI36
NG_012848.1:g.6915C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000639438.3:c.506C>T MANE Select	ENSP00000491782.1:p.Thr169Ile
ENST00000338516.7:c.506C>T	ENSP00000344297.4:p.Thr169Ile
ENST00000341640.6:c.482C>T	ENSP00000339906.2:p.Thr161Ile
ENST00000378740.6:c.482C>T	ENSP00000368014.3:p.Thr161Ile
ENST00000463946.5:c.476C>T	ENSP00000451923.1:p.Thr159Ile
ENST00000477423.1:n.476C>T
ENST00000483494.5:c.476C>T	ENSP00000473846.1:p.Thr159Ile
ENST00000611453.1:c.476C>T	ENSP00000477877.1:p.Thr159Ile
NM_006193.2:c.482C>T	NP_006184.2:p.Thr161Ile
XM_011516276.1:c.506C>T	XP_011514578.1:p.Thr169Ile
NM_001366110.1:c.506C>T MANE Select	NP_001353039.1:p.Thr169Ile
NM_001366111.1:c.506C>T	NP_001353040.1:p.Thr169Ile