Canonical Allele Identifier: CA18646761

Gene: PADI4

Linked Data

• dbSNP Id: rs902236376
• gnomAD v4: 1-17346164-G-C
• MyVariant Identifiers: chr1:g.17672659G>C (hg19) ; chr1:g.17346164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346164G>C , CM000663.2:g.17346164G>C	GRCh38
NC_000001.10:g.17672659G>C , CM000663.1:g.17672659G>C	GRCh37
NC_000001.9:g.17545246G>C	NCBI36
NG_023261.2:g.42975G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1047+25G>C MANE Select	ENSP00000364597.4:n.1047+25G>C
ENST00000468945.1:n.106+25G>C
NM_012387.2:c.1047+25G>C	NP_036519.2:n.1047+25G>C
XM_011541150.1:c.861+25G>C	XP_011539452.1:n.861+25G>C
XM_011541151.1:c.1047+25G>C	XP_011539453.1:n.1047+25G>C
XM_011541152.1:c.510+25G>C	XP_011539454.1:n.510+25G>C
XM_011541153.1:c.1047+25G>C	XP_011539455.1:n.1047+25G>C
XM_011541154.1:c.1047+25G>C	XP_011539456.1:n.1047+25G>C
XM_011541155.1:c.1047+25G>C	XP_011539457.1:n.1047+25G>C
XM_011541156.1:c.1047+25G>C	XP_011539458.1:n.1047+25G>C
XM_011541157.1:c.156+25G>C	XP_011539459.1:n.156+25G>C
XM_011541154.2:c.1047+25G>C	XP_011539456.1:n.1047+25G>C
NM_012387.3:c.1047+25G>C MANE Select	NP_036519.2:n.1047+25G>C