Canonical Allele Identifier: CA2574237535
Gene: PADI4 HGNC NCBI

Linked Data

gnomAD v4: 1-17336263-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336263T>A , CM000663.2:g.17336263T>A GRCh38
NC_000001.10:g.17662758T>A , CM000663.1:g.17662758T>A GRCh37
NC_000001.9:g.17535345T>A NCBI36
NG_023261.2:g.33074T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.408+37T>A MANE Select ENSP00000364597.4:n.408+37T>A
NM_012387.2:c.408+37T>A NP_036519.2:n.408+37T>A
XM_011541150.1:c.340+2254T>A XP_011539452.1:n.340+2254T>A
XM_011541151.1:c.408+37T>A XP_011539453.1:n.408+37T>A
XM_011541152.1:c.-12+37T>A XP_011539454.1:n.-12+37T>A
XM_011541153.1:c.408+37T>A XP_011539455.1:n.408+37T>A
XM_011541154.1:c.408+37T>A XP_011539456.1:n.408+37T>A
XM_011541155.1:c.408+37T>A XP_011539457.1:n.408+37T>A
XM_011541156.1:c.408+37T>A XP_011539458.1:n.408+37T>A
XM_011541157.1:c.-305+37T>A XP_011539459.1:n.-305+37T>A
XM_011541154.2:c.408+37T>A XP_011539456.1:n.408+37T>A
NM_012387.3:c.408+37T>A MANE Select NP_036519.2:n.408+37T>A