Canonical Allele Identifier: CA2643694290
Gene: PADI4 HGNC NCBI

Linked Data

gnomAD v4: 1-17347859-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347859T>G , CM000663.2:g.17347859T>G GRCh38
NC_000001.10:g.17674354T>G , CM000663.1:g.17674354T>G GRCh37
NC_000001.9:g.17546941T>G NCBI36
NG_023261.2:g.44670T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1048-82T>G MANE Select ENSP00000364597.4:n.1048-82T>G
ENST00000468945.1:n.107-82T>G
NM_012387.2:c.1048-82T>G NP_036519.2:n.1048-82T>G
XM_011541150.1:c.862-82T>G XP_011539452.1:n.862-82T>G
XM_011541151.1:c.1048-82T>G XP_011539453.1:n.1048-82T>G
XM_011541152.1:c.511-82T>G XP_011539454.1:n.511-82T>G
XM_011541153.1:c.1048-82T>G XP_011539455.1:n.1048-82T>G
XM_011541154.1:c.1048-82T>G XP_011539456.1:n.1048-82T>G
XM_011541155.1:c.1048-82T>G XP_011539457.1:n.1048-82T>G
XM_011541156.1:c.1048-82T>G XP_011539458.1:n.1048-82T>G
XM_011541157.1:c.157-82T>G XP_011539459.1:n.157-82T>G
XM_011541154.2:c.1048-82T>G XP_011539456.1:n.1048-82T>G
NM_012387.3:c.1048-82T>G MANE Select NP_036519.2:n.1048-82T>G