Canonical Allele Identifier: CA10662267

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17338906G>A , CM000663.2:g.17338906G>A	GRCh38
NC_000001.10:g.17665401G>A , CM000663.1:g.17665401G>A	GRCh37
NC_000001.9:g.17537988G>A	NCBI36
NG_023261.2:g.35717G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012387.3:c.526+751G>A MANE Select	NP_036519.2:n.526+751G>A
ENST00000375448.4:c.526+751G>A MANE Select	ENSP00000364597.4:n.526+751G>A
NM_012387.2:c.526+751G>A	NP_036519.2:n.526+751G>A
XM_011541150.1:c.341-782G>A	XP_011539452.1:n.341-782G>A
XM_011541151.1:c.526+751G>A	XP_011539453.1:n.526+751G>A
XM_011541152.1:c.-11-782G>A	XP_011539454.1:n.-11-782G>A
XM_011541153.1:c.526+751G>A	XP_011539455.1:n.526+751G>A
XM_011541154.1:c.526+751G>A	XP_011539456.1:n.526+751G>A
XM_011541154.2:c.526+751G>A	XP_011539456.1:n.526+751G>A
XM_011541155.1:c.526+751G>A	XP_011539457.1:n.526+751G>A
XM_011541156.1:c.526+751G>A	XP_011539458.1:n.526+751G>A
XM_011541157.1:c.-187+751G>A	XP_011539459.1:n.-187+751G>A