Canonical Allele Identifier: CA640731

Gene: PADI4

Linked Data

• dbSNP Id: rs768187144
• ExAC: 1:17672502 C / G
• gnomAD v2: 1-17672502-C-G
• gnomAD v4: 1-17346007-C-G
• MyVariant Identifiers: chr1:g.17672502C>G (hg19) ; chr1:g.17346007C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346007C>G , CM000663.2:g.17346007C>G	GRCh38
NC_000001.10:g.17672502C>G , CM000663.1:g.17672502C>G	GRCh37
NC_000001.9:g.17545089C>G	NCBI36
NG_023261.2:g.42818C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.936-21C>G MANE Select	ENSP00000364597.4:n.936-21C>G
NM_012387.2:c.936-21C>G	NP_036519.2:n.936-21C>G
XM_011541150.1:c.750-21C>G	XP_011539452.1:n.750-21C>G
XM_011541151.1:c.936-21C>G	XP_011539453.1:n.936-21C>G
XM_011541152.1:c.399-21C>G	XP_011539454.1:n.399-21C>G
XM_011541153.1:c.936-21C>G	XP_011539455.1:n.936-21C>G
XM_011541154.1:c.936-21C>G	XP_011539456.1:n.936-21C>G
XM_011541155.1:c.936-21C>G	XP_011539457.1:n.936-21C>G
XM_011541156.1:c.936-21C>G	XP_011539458.1:n.936-21C>G
XM_011541157.1:c.45-21C>G	XP_011539459.1:n.45-21C>G
XM_011541154.2:c.936-21C>G	XP_011539456.1:n.936-21C>G
NM_012387.3:c.936-21C>G MANE Select	NP_036519.2:n.936-21C>G