Canonical Allele Identifier: CA891204093

Gene: PADI4

Linked Data

• dbSNP Id: rs1312695364
• gnomAD v3: 1-17333849-CCAGTGCCCTA-C
• gnomAD v4: 1-17333849-CCAGTGCCCTA-C
• MyVariant Identifiers: chr1:g.17333850_17333859del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17333851_17333860del , CM000663.2:g.17333851_17333860del	GRCh38
NC_000001.10:g.17660346_17660355del , CM000663.1:g.17660346_17660355del	GRCh37
NC_000001.9:g.17532933_17532942del	NCBI36
NG_023261.2:g.30662_30671del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.274-92_274-83del MANE Select	ENSP00000364597.4:n.274-92_274-83del
ENST00000375453.5:c.274-92_274-83del	ENSP00000364602.1:n.274-92_274-83del
NM_012387.2:c.274-92_274-83del	NP_036519.2:n.274-92_274-83del
XM_011541150.1:c.274-92_274-83del	XP_011539452.1:n.274-92_274-83del
XM_011541151.1:c.274-92_274-83del	XP_011539453.1:n.274-92_274-83del
XM_011541153.1:c.274-92_274-83del	XP_011539455.1:n.274-92_274-83del
XM_011541154.1:c.274-92_274-83del	XP_011539456.1:n.274-92_274-83del
XM_011541155.1:c.274-92_274-83del	XP_011539457.1:n.274-92_274-83del
XM_011541156.1:c.274-92_274-83del	XP_011539458.1:n.274-92_274-83del
XM_011541154.2:c.274-92_274-83del	XP_011539456.1:n.274-92_274-83del
NM_012387.3:c.274-92_274-83del MANE Select	NP_036519.2:n.274-92_274-83del