Canonical Allele Identifier: CA2643699234
Gene: PADI4 HGNC NCBI

Linked Data

gnomAD v4: 1-17336262-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336262C>A , CM000663.2:g.17336262C>A GRCh38
NC_000001.10:g.17662757C>A , CM000663.1:g.17662757C>A GRCh37
NC_000001.9:g.17535344C>A NCBI36
NG_023261.2:g.33073C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.408+36C>A MANE Select ENSP00000364597.4:n.408+36C>A
NM_012387.2:c.408+36C>A NP_036519.2:n.408+36C>A
XM_011541150.1:c.340+2253C>A XP_011539452.1:n.340+2253C>A
XM_011541151.1:c.408+36C>A XP_011539453.1:n.408+36C>A
XM_011541152.1:c.-12+36C>A XP_011539454.1:n.-12+36C>A
XM_011541153.1:c.408+36C>A XP_011539455.1:n.408+36C>A
XM_011541154.1:c.408+36C>A XP_011539456.1:n.408+36C>A
XM_011541155.1:c.408+36C>A XP_011539457.1:n.408+36C>A
XM_011541156.1:c.408+36C>A XP_011539458.1:n.408+36C>A
XM_011541157.1:c.-305+36C>A XP_011539459.1:n.-305+36C>A
XM_011541154.2:c.408+36C>A XP_011539456.1:n.408+36C>A
NM_012387.3:c.408+36C>A MANE Select NP_036519.2:n.408+36C>A
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