Canonical Allele Identifier: CA1156199737
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347787_17347788delinsTC , CM000663.2:g.17347787_17347788delinsTC GRCh38
NC_000001.10:g.17674282_17674283delinsTC , CM000663.1:g.17674282_17674283delinsTC GRCh37
NC_000001.9:g.17546869_17546870delinsTC NCBI36
NG_023261.2:g.44598_44599delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1048-154_1048-153delinsTC MANE Select ENSP00000364597.4:n.1048-154_1048-153delinsTC
ENST00000468945.1:n.107-154_107-153delinsTC
NM_012387.2:c.1048-154_1048-153delinsTC NP_036519.2:n.1048-154_1048-153delinsTC
XM_011541150.1:c.862-154_862-153delinsTC XP_011539452.1:n.862-154_862-153delinsTC
XM_011541151.1:c.1048-154_1048-153delinsTC XP_011539453.1:n.1048-154_1048-153delinsTC
XM_011541152.1:c.511-154_511-153delinsTC XP_011539454.1:n.511-154_511-153delinsTC
XM_011541153.1:c.1048-154_1048-153delinsTC XP_011539455.1:n.1048-154_1048-153delinsTC
XM_011541154.1:c.1048-154_1048-153delinsTC XP_011539456.1:n.1048-154_1048-153delinsTC
XM_011541155.1:c.1048-154_1048-153delinsTC XP_011539457.1:n.1048-154_1048-153delinsTC
XM_011541156.1:c.1048-154_1048-153delinsTC XP_011539458.1:n.1048-154_1048-153delinsTC
XM_011541157.1:c.157-154_157-153delinsTC XP_011539459.1:n.157-154_157-153delinsTC
XM_011541154.2:c.1048-154_1048-153delinsTC XP_011539456.1:n.1048-154_1048-153delinsTC
NM_012387.3:c.1048-154_1048-153delinsTC MANE Select NP_036519.2:n.1048-154_1048-153delinsTC