Canonical Allele Identifier: CA640409

Gene: PADI4

Linked Data

• dbSNP Id: rs749986382
• ExAC: 1:17660486 C / G
• gnomAD v2: 1-17660486-C-G
• MyVariant Identifiers: chr1:g.17660486C>G (hg19) ; chr1:g.17333991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17333991C>G , CM000663.2:g.17333991C>G	GRCh38
NC_000001.10:g.17660486C>G , CM000663.1:g.17660486C>G	GRCh37
NC_000001.9:g.17533073C>G	NCBI36
NG_023261.2:g.30802C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.322C>G MANE Select	ENSP00000364597.4:p.Leu108Val
ENST00000375453.5:c.322C>G	ENSP00000364602.1:p.Leu108Val
NM_012387.2:c.322C>G	NP_036519.2:p.Leu108Val
XM_011541150.1:c.322C>G	XP_011539452.1:p.Leu108Val
XM_011541151.1:c.322C>G	XP_011539453.1:p.Leu108Val
XM_011541153.1:c.322C>G	XP_011539455.1:p.Leu108Val
XM_011541154.1:c.322C>G	XP_011539456.1:p.Leu108Val
XM_011541155.1:c.322C>G	XP_011539457.1:p.Leu108Val
XM_011541156.1:c.322C>G	XP_011539458.1:p.Leu108Val
XM_011541157.1:c.-391C>G	XP_011539459.1:n.-391C>G
XM_011541154.2:c.322C>G	XP_011539456.1:p.Leu108Val
NM_012387.3:c.322C>G MANE Select	NP_036519.2:p.Leu108Val