Canonical Allele Identifier: CA1156187246

Gene: PADI4

Linked Data

• dbSNP Id: rs1570037072
• gnomAD v4: 1-17336258-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336258T>C , CM000663.2:g.17336258T>C	GRCh38
NC_000001.10:g.17662753T>C , CM000663.1:g.17662753T>C	GRCh37
NC_000001.9:g.17535340T>C	NCBI36
NG_023261.2:g.33069T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.408+32T>C MANE Select	ENSP00000364597.4:n.408+32T>C
NM_012387.2:c.408+32T>C	NP_036519.2:n.408+32T>C
XM_011541150.1:c.340+2249T>C	XP_011539452.1:n.340+2249T>C
XM_011541151.1:c.408+32T>C	XP_011539453.1:n.408+32T>C
XM_011541152.1:c.-12+32T>C	XP_011539454.1:n.-12+32T>C
XM_011541153.1:c.408+32T>C	XP_011539455.1:n.408+32T>C
XM_011541154.1:c.408+32T>C	XP_011539456.1:n.408+32T>C
XM_011541155.1:c.408+32T>C	XP_011539457.1:n.408+32T>C
XM_011541156.1:c.408+32T>C	XP_011539458.1:n.408+32T>C
XM_011541157.1:c.-305+32T>C	XP_011539459.1:n.-305+32T>C
XM_011541154.2:c.408+32T>C	XP_011539456.1:n.408+32T>C
NM_012387.3:c.408+32T>C MANE Select	NP_036519.2:n.408+32T>C