Canonical Allele Identifier: CA1156187254

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336263_17336264delinsTG , CM000663.2:g.17336263_17336264delinsTG	GRCh38
NC_000001.10:g.17662758_17662759delinsTG , CM000663.1:g.17662758_17662759delinsTG	GRCh37
NC_000001.9:g.17535345_17535346delinsTG	NCBI36
NG_023261.2:g.33074_33075delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.408+37_408+38delinsTG MANE Select	ENSP00000364597.4:n.408+37_408+38delinsTG...
NM_012387.2:c.408+37_408+38delinsTG	NP_036519.2:n.408+37_408+38delinsTG
XM_011541150.1:c.340+2254_340+2255delinsTG	XP_011539452.1:n.340+2254_340+2255delinsT...
XM_011541151.1:c.408+37_408+38delinsTG	XP_011539453.1:n.408+37_408+38delinsTG
XM_011541152.1:c.-12+37_-12+38delinsTG	XP_011539454.1:n.-12+37_-12+38delinsTG
XM_011541153.1:c.408+37_408+38delinsTG	XP_011539455.1:n.408+37_408+38delinsTG
XM_011541154.1:c.408+37_408+38delinsTG	XP_011539456.1:n.408+37_408+38delinsTG
XM_011541155.1:c.408+37_408+38delinsTG	XP_011539457.1:n.408+37_408+38delinsTG
XM_011541156.1:c.408+37_408+38delinsTG	XP_011539458.1:n.408+37_408+38delinsTG
XM_011541157.1:c.-305+37_-305+38delinsTG	XP_011539459.1:n.-305+37_-305+38delinsTG
XM_011541154.2:c.408+37_408+38delinsTG	XP_011539456.1:n.408+37_408+38delinsTG
NM_012387.3:c.408+37_408+38delinsTG MANE Select	NP_036519.2:n.408+37_408+38delinsTG