Canonical Allele Identifier: CA18648322

Gene: PADI4

Linked Data

• dbSNP Id: rs910470150
• gnomAD v3: 1-17348064-G-T
• gnomAD v4: 1-17348064-G-T
• MyVariant Identifiers: chr1:g.17674559G>T (hg19) ; chr1:g.17348064G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348064G>T , CM000663.2:g.17348064G>T	GRCh38
NC_000001.10:g.17674559G>T , CM000663.1:g.17674559G>T	GRCh37
NC_000001.9:g.17547146G>T	NCBI36
NG_023261.2:g.44875G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+16G>T MANE Select	ENSP00000364597.4:n.1155+16G>T
ENST00000468945.1:n.230G>T
ENST00000487048.5:n.122+16G>T
NM_012387.2:c.1155+16G>T	NP_036519.2:n.1155+16G>T
XM_011541150.1:c.969+16G>T	XP_011539452.1:n.969+16G>T
XM_011541151.1:c.1155+16G>T	XP_011539453.1:n.1155+16G>T
XM_011541152.1:c.618+16G>T	XP_011539454.1:n.618+16G>T
XM_011541153.1:c.1155+16G>T	XP_011539455.1:n.1155+16G>T
XM_011541154.1:c.1155+16G>T	XP_011539456.1:n.1155+16G>T
XM_011541155.1:c.1155+16G>T	XP_011539457.1:n.1155+16G>T
XM_011541156.1:c.1155+16G>T	XP_011539458.1:n.1155+16G>T
XM_011541157.1:c.264+16G>T	XP_011539459.1:n.264+16G>T
XM_011541154.2:c.1155+16G>T	XP_011539456.1:n.1155+16G>T
NM_012387.3:c.1155+16G>T MANE Select	NP_036519.2:n.1155+16G>T