Canonical Allele Identifier: CA640503

Gene: PADI4

Linked Data

• dbSNP Id: rs760590796
• ExAC: 1:17662758 TG / T
• gnomAD v2: 1-17662758-TG-T
• gnomAD v4: 1-17336263-TG-T
• MyVariant Identifiers: chr1:g.17662759del (hg19) ; chr1:g.17336264del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336265del , CM000663.2:g.17336265del	GRCh38
NC_000001.10:g.17662760del , CM000663.1:g.17662760del	GRCh37
NC_000001.9:g.17535347del	NCBI36
NG_023261.2:g.33076del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.408+39del MANE Select	ENSP00000364597.4:n.408+39del
NM_012387.2:c.408+39del	NP_036519.2:n.408+39del
XM_011541150.1:c.340+2256del	XP_011539452.1:n.340+2256del
XM_011541151.1:c.408+39del	XP_011539453.1:n.408+39del
XM_011541152.1:c.-12+39del	XP_011539454.1:n.-12+39del
XM_011541153.1:c.408+39del	XP_011539455.1:n.408+39del
XM_011541154.1:c.408+39del	XP_011539456.1:n.408+39del
XM_011541155.1:c.408+39del	XP_011539457.1:n.408+39del
XM_011541156.1:c.408+39del	XP_011539458.1:n.408+39del
XM_011541157.1:c.-305+39del	XP_011539459.1:n.-305+39del
XM_011541154.2:c.408+39del	XP_011539456.1:n.408+39del
NM_012387.3:c.408+39del MANE Select	NP_036519.2:n.408+39del