Canonical Allele Identifier: CA521046650

Gene: PADI4

Linked Data

• dbSNP Id: rs1234585557
• gnomAD v2: 1-17674365-CCCCATCCTGGCG-C
• gnomAD v3: 1-17347870-CCCCATCCTGGCG-C
• gnomAD v4: 1-17347870-CCCCATCCTGGCG-C
• MyVariant Identifiers: chr1:g.17674366_17674377del (hg19) ; chr1:g.17347871_17347882del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347871_17347882del , CM000663.2:g.17347871_17347882del	GRCh38
NC_000001.10:g.17674366_17674377del , CM000663.1:g.17674366_17674377del	GRCh37
NC_000001.9:g.17546953_17546964del	NCBI36
NG_023261.2:g.44682_44693del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1048-70_1048-59del MANE Select	ENSP00000364597.4:n.1048-70_1048-59del
ENST00000468945.1:n.107-70_107-59del
NM_012387.2:c.1048-70_1048-59del	NP_036519.2:n.1048-70_1048-59del
XM_011541150.1:c.862-70_862-59del	XP_011539452.1:n.862-70_862-59del
XM_011541151.1:c.1048-70_1048-59del	XP_011539453.1:n.1048-70_1048-59del
XM_011541152.1:c.511-70_511-59del	XP_011539454.1:n.511-70_511-59del
XM_011541153.1:c.1048-70_1048-59del	XP_011539455.1:n.1048-70_1048-59del
XM_011541154.1:c.1048-70_1048-59del	XP_011539456.1:n.1048-70_1048-59del
XM_011541155.1:c.1048-70_1048-59del	XP_011539457.1:n.1048-70_1048-59del
XM_011541156.1:c.1048-70_1048-59del	XP_011539458.1:n.1048-70_1048-59del
XM_011541157.1:c.157-70_157-59del	XP_011539459.1:n.157-70_157-59del
XM_011541154.2:c.1048-70_1048-59del	XP_011539456.1:n.1048-70_1048-59del
NM_012387.3:c.1048-70_1048-59del MANE Select	NP_036519.2:n.1048-70_1048-59del