Canonical Allele Identifier: CA2643698430

Gene: PADI4

Linked Data

• gnomAD v4: 1-17334180-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334180T>C , CM000663.2:g.17334180T>C	GRCh38
NC_000001.10:g.17660675T>C , CM000663.1:g.17660675T>C	GRCh37
NC_000001.9:g.17533262T>C	NCBI36
NG_023261.2:g.30991T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.340+171T>C MANE Select	ENSP00000364597.4:n.340+171T>C
ENST00000375453.5:c.341-144T>C	ENSP00000364602.1:n.341-144T>C
NM_012387.2:c.340+171T>C	NP_036519.2:n.340+171T>C
XM_011541150.1:c.340+171T>C	XP_011539452.1:n.340+171T>C
XM_011541151.1:c.340+171T>C	XP_011539453.1:n.340+171T>C
XM_011541152.1:c.-80+171T>C	XP_011539454.1:n.-80+171T>C
XM_011541153.1:c.340+171T>C	XP_011539455.1:n.340+171T>C
XM_011541154.1:c.340+171T>C	XP_011539456.1:n.340+171T>C
XM_011541155.1:c.340+171T>C	XP_011539457.1:n.340+171T>C
XM_011541156.1:c.340+171T>C	XP_011539458.1:n.340+171T>C
XM_011541157.1:c.-373+171T>C	XP_011539459.1:n.-373+171T>C
XM_011541154.2:c.340+171T>C	XP_011539456.1:n.340+171T>C
NM_012387.3:c.340+171T>C MANE Select	NP_036519.2:n.340+171T>C