Canonical Allele Identifier: CA2643694398

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348056-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348056C>A , CM000663.2:g.17348056C>A	GRCh38
NC_000001.10:g.17674551C>A , CM000663.1:g.17674551C>A	GRCh37
NC_000001.9:g.17547138C>A	NCBI36
NG_023261.2:g.44867C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+8C>A MANE Select	ENSP00000364597.4:n.1155+8C>A
ENST00000468945.1:n.222C>A
ENST00000487048.5:n.122+8C>A
NM_012387.2:c.1155+8C>A	NP_036519.2:n.1155+8C>A
XM_011541150.1:c.969+8C>A	XP_011539452.1:n.969+8C>A
XM_011541151.1:c.1155+8C>A	XP_011539453.1:n.1155+8C>A
XM_011541152.1:c.618+8C>A	XP_011539454.1:n.618+8C>A
XM_011541153.1:c.1155+8C>A	XP_011539455.1:n.1155+8C>A
XM_011541154.1:c.1155+8C>A	XP_011539456.1:n.1155+8C>A
XM_011541155.1:c.1155+8C>A	XP_011539457.1:n.1155+8C>A
XM_011541156.1:c.1155+8C>A	XP_011539458.1:n.1155+8C>A
XM_011541157.1:c.264+8C>A	XP_011539459.1:n.264+8C>A
XM_011541154.2:c.1155+8C>A	XP_011539456.1:n.1155+8C>A
NM_012387.3:c.1155+8C>A MANE Select	NP_036519.2:n.1155+8C>A