Canonical Allele Identifier: CA2643698301

Gene: PADI4

Linked Data

• gnomAD v4: 1-17334004-G-GTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334004_17334005insTGA , CM000663.2:g.17334004_17334005insTGA	GRCh38
NC_000001.10:g.17660499_17660500insTGA , CM000663.1:g.17660499_17660500insTGA	GRCh37
NC_000001.9:g.17533086_17533087insTGA	NCBI36
NG_023261.2:g.30815_30816insTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.335_336insTGA MANE Select	ENSP00000364597.4:p.Gly112_Val113insGlu
ENST00000375453.5:c.335_336insTGA	ENSP00000364602.1:p.Gly112_Val113insGlu
NM_012387.2:c.335_336insTGA	NP_036519.2:p.Gly112_Val113insGlu
XM_011541150.1:c.335_336insTGA	XP_011539452.1:p.Gly112_Val113insGlu
XM_011541151.1:c.335_336insTGA	XP_011539453.1:p.Gly112_Val113insGlu
XM_011541152.1:c.-85_-84insTGA	XP_011539454.1:n.-85_-84insTGA
XM_011541153.1:c.335_336insTGA	XP_011539455.1:p.Gly112_Val113insGlu
XM_011541154.1:c.335_336insTGA	XP_011539456.1:p.Gly112_Val113insGlu
XM_011541155.1:c.335_336insTGA	XP_011539457.1:p.Gly112_Val113insGlu
XM_011541156.1:c.335_336insTGA	XP_011539458.1:p.Gly112_Val113insGlu
XM_011541157.1:c.-378_-377insTGA	XP_011539459.1:n.-378_-377insTGA
XM_011541154.2:c.335_336insTGA	XP_011539456.1:p.Gly112_Val113insGlu
NM_012387.3:c.335_336insTGA MANE Select	NP_036519.2:p.Gly112_Val113insGlu