Canonical Allele Identifier: CA2643694229

Gene: PADI4

Linked Data

• gnomAD v4: 1-17347797-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347801_17347802del , CM000663.2:g.17347801_17347802del	GRCh38
NC_000001.10:g.17674296_17674297del , CM000663.1:g.17674296_17674297del	GRCh37
NC_000001.9:g.17546883_17546884del	NCBI36
NG_023261.2:g.44612_44613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1048-140_1048-139del MANE Select	ENSP00000364597.4:n.1048-140_1048-139del
ENST00000468945.1:n.107-140_107-139del
NM_012387.2:c.1048-140_1048-139del	NP_036519.2:n.1048-140_1048-139del
XM_011541150.1:c.862-140_862-139del	XP_011539452.1:n.862-140_862-139del
XM_011541151.1:c.1048-140_1048-139del	XP_011539453.1:n.1048-140_1048-139del
XM_011541152.1:c.511-140_511-139del	XP_011539454.1:n.511-140_511-139del
XM_011541153.1:c.1048-140_1048-139del	XP_011539455.1:n.1048-140_1048-139del
XM_011541154.1:c.1048-140_1048-139del	XP_011539456.1:n.1048-140_1048-139del
XM_011541155.1:c.1048-140_1048-139del	XP_011539457.1:n.1048-140_1048-139del
XM_011541156.1:c.1048-140_1048-139del	XP_011539458.1:n.1048-140_1048-139del
XM_011541157.1:c.157-140_157-139del	XP_011539459.1:n.157-140_157-139del
XM_011541154.2:c.1048-140_1048-139del	XP_011539456.1:n.1048-140_1048-139del
NM_012387.3:c.1048-140_1048-139del MANE Select	NP_036519.2:n.1048-140_1048-139del