Canonical Allele Identifier: CA521046683

Gene: PADI4

Linked Data

• dbSNP Id: rs1190316143
• gnomAD v2: 1-17674549-T-A
• gnomAD v4: 1-17348054-T-A
• MyVariant Identifiers: chr1:g.17674549T>A (hg19) ; chr1:g.17348054T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348054T>A , CM000663.2:g.17348054T>A	GRCh38
NC_000001.10:g.17674549T>A , CM000663.1:g.17674549T>A	GRCh37
NC_000001.9:g.17547136T>A	NCBI36
NG_023261.2:g.44865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+6T>A MANE Select	ENSP00000364597.4:n.1155+6T>A
ENST00000468945.1:n.220T>A
ENST00000487048.5:n.122+6T>A
NM_012387.2:c.1155+6T>A	NP_036519.2:n.1155+6T>A
XM_011541150.1:c.969+6T>A	XP_011539452.1:n.969+6T>A
XM_011541151.1:c.1155+6T>A	XP_011539453.1:n.1155+6T>A
XM_011541152.1:c.618+6T>A	XP_011539454.1:n.618+6T>A
XM_011541153.1:c.1155+6T>A	XP_011539455.1:n.1155+6T>A
XM_011541154.1:c.1155+6T>A	XP_011539456.1:n.1155+6T>A
XM_011541155.1:c.1155+6T>A	XP_011539457.1:n.1155+6T>A
XM_011541156.1:c.1155+6T>A	XP_011539458.1:n.1155+6T>A
XM_011541157.1:c.264+6T>A	XP_011539459.1:n.264+6T>A
XM_011541154.2:c.1155+6T>A	XP_011539456.1:n.1155+6T>A
NM_012387.3:c.1155+6T>A MANE Select	NP_036519.2:n.1155+6T>A