Canonical Allele Identifier: CA891204358

Gene: PADI4

Linked Data

• dbSNP Id: rs975403608
• gnomAD v3: 1-17334208-G-C
• gnomAD v4: 1-17334208-G-C
• MyVariant Identifiers: chr1:g.17660703G>C (hg19) ; chr1:g.17334208G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334208G>C , CM000663.2:g.17334208G>C	GRCh38
NC_000001.10:g.17660703G>C , CM000663.1:g.17660703G>C	GRCh37
NC_000001.9:g.17533290G>C	NCBI36
NG_023261.2:g.31019G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.340+199G>C MANE Select	ENSP00000364597.4:n.340+199G>C
ENST00000375453.5:c.341-116G>C	ENSP00000364602.1:n.341-116G>C
NM_012387.2:c.340+199G>C	NP_036519.2:n.340+199G>C
XM_011541150.1:c.340+199G>C	XP_011539452.1:n.340+199G>C
XM_011541151.1:c.340+199G>C	XP_011539453.1:n.340+199G>C
XM_011541152.1:c.-80+199G>C	XP_011539454.1:n.-80+199G>C
XM_011541153.1:c.340+199G>C	XP_011539455.1:n.340+199G>C
XM_011541154.1:c.340+199G>C	XP_011539456.1:n.340+199G>C
XM_011541155.1:c.340+199G>C	XP_011539457.1:n.340+199G>C
XM_011541156.1:c.340+199G>C	XP_011539458.1:n.340+199G>C
XM_011541157.1:c.-373+199G>C	XP_011539459.1:n.-373+199G>C
XM_011541154.2:c.340+199G>C	XP_011539456.1:n.340+199G>C
NM_012387.3:c.340+199G>C MANE Select	NP_036519.2:n.340+199G>C