Canonical Allele Identifier: CA640500
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs1621005
gnomAD v2: 1-17662751-C-G
gnomAD v3: 1-17336256-C-G
gnomAD v4: 1-17336256-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336256C>G , CM000663.2:g.17336256C>G GRCh38
NC_000001.10:g.17662751C>G , CM000663.1:g.17662751C>G GRCh37
NC_000001.9:g.17535338C>G NCBI36
NG_023261.2:g.33067C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.408+30C>G MANE Select ENSP00000364597.4:n.408+30C>G
NM_012387.2:c.408+30C>G NP_036519.2:n.408+30C>G
XM_011541150.1:c.340+2247C>G XP_011539452.1:n.340+2247C>G
XM_011541151.1:c.408+30C>G XP_011539453.1:n.408+30C>G
XM_011541152.1:c.-12+30C>G XP_011539454.1:n.-12+30C>G
XM_011541153.1:c.408+30C>G XP_011539455.1:n.408+30C>G
XM_011541154.1:c.408+30C>G XP_011539456.1:n.408+30C>G
XM_011541155.1:c.408+30C>G XP_011539457.1:n.408+30C>G
XM_011541156.1:c.408+30C>G XP_011539458.1:n.408+30C>G
XM_011541157.1:c.-305+30C>G XP_011539459.1:n.-305+30C>G
XM_011541154.2:c.408+30C>G XP_011539456.1:n.408+30C>G
NM_012387.3:c.408+30C>G MANE Select NP_036519.2:n.408+30C>G