Canonical Allele Identifier: CA1156197973

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346154_17346158delinsGGGCA , CM000663.2:g.17346154_17346158delinsGGGCA	GRCh38
NC_000001.10:g.17672649_17672653delinsGGGCA , CM000663.1:g.17672649_17672653delinsGGGCA	GRCh37
NC_000001.9:g.17545236_17545240delinsGGGCA	NCBI36
NG_023261.2:g.42965_42969delinsGGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1047+15_1047+19delinsGGGCA MANE Select	ENSP00000364597.4:n.1047+15_1047+19delinsGGGCA
ENST00000468945.1:n.106+15_106+19delinsGGGCA
NM_012387.2:c.1047+15_1047+19delinsGGGCA	NP_036519.2:n.1047+15_1047+19delinsGGGCA
XM_011541150.1:c.861+15_861+19delinsGGGCA	XP_011539452.1:n.861+15_861+19delinsGGGCA
XM_011541151.1:c.1047+15_1047+19delinsGGGCA	XP_011539453.1:n.1047+15_1047+19delinsGGGCA
XM_011541152.1:c.510+15_510+19delinsGGGCA	XP_011539454.1:n.510+15_510+19delinsGGGCA
XM_011541153.1:c.1047+15_1047+19delinsGGGCA	XP_011539455.1:n.1047+15_1047+19delinsGGGCA
XM_011541154.1:c.1047+15_1047+19delinsGGGCA	XP_011539456.1:n.1047+15_1047+19delinsGGGCA
XM_011541155.1:c.1047+15_1047+19delinsGGGCA	XP_011539457.1:n.1047+15_1047+19delinsGGGCA
XM_011541156.1:c.1047+15_1047+19delinsGGGCA	XP_011539458.1:n.1047+15_1047+19delinsGGGCA
XM_011541157.1:c.156+15_156+19delinsGGGCA	XP_011539459.1:n.156+15_156+19delinsGGGCA
XM_011541154.2:c.1047+15_1047+19delinsGGGCA	XP_011539456.1:n.1047+15_1047+19delinsGGGCA
NM_012387.3:c.1047+15_1047+19delinsGGGCA MANE Select	NP_036519.2:n.1047+15_1047+19delinsGGGCA