Canonical Allele Identifier: CA1156199963

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347933_17347934delinsTC , CM000663.2:g.17347933_17347934delinsTC	GRCh38
NC_000001.10:g.17674428_17674429delinsTC , CM000663.1:g.17674428_17674429delinsTC	GRCh37
NC_000001.9:g.17547015_17547016delinsTC	NCBI36
NG_023261.2:g.44744_44745delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1048-8_1048-7delinsTC MANE Select	ENSP00000364597.4:n.1048-8_1048-7delinsTC
ENST00000468945.1:n.107-8_107-7delinsTC
ENST00000487048.5:n.7_8delinsTC
NM_012387.2:c.1048-8_1048-7delinsTC	NP_036519.2:n.1048-8_1048-7delinsTC
XM_011541150.1:c.862-8_862-7delinsTC	XP_011539452.1:n.862-8_862-7delinsTC
XM_011541151.1:c.1048-8_1048-7delinsTC	XP_011539453.1:n.1048-8_1048-7delinsTC
XM_011541152.1:c.511-8_511-7delinsTC	XP_011539454.1:n.511-8_511-7delinsTC
XM_011541153.1:c.1048-8_1048-7delinsTC	XP_011539455.1:n.1048-8_1048-7delinsTC
XM_011541154.1:c.1048-8_1048-7delinsTC	XP_011539456.1:n.1048-8_1048-7delinsTC
XM_011541155.1:c.1048-8_1048-7delinsTC	XP_011539457.1:n.1048-8_1048-7delinsTC
XM_011541156.1:c.1048-8_1048-7delinsTC	XP_011539458.1:n.1048-8_1048-7delinsTC
XM_011541157.1:c.157-8_157-7delinsTC	XP_011539459.1:n.157-8_157-7delinsTC
XM_011541154.2:c.1048-8_1048-7delinsTC	XP_011539456.1:n.1048-8_1048-7delinsTC
NM_012387.3:c.1048-8_1048-7delinsTC MANE Select	NP_036519.2:n.1048-8_1048-7delinsTC