Canonical Allele Identifier: CA416400953
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17657626T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17331131T>C , CM000663.2:g.17331131T>C GRCh38
NC_000001.10:g.17657626T>C , CM000663.1:g.17657626T>C GRCh37
NC_000001.9:g.17530213T>C NCBI36
NG_023261.2:g.27942T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.255T>C MANE Select ENSP00000364597.4:p.Gly85=
ENST00000375453.5:c.255T>C ENSP00000364602.1:p.Gly85=
ENST00000624583.1:c.166+500A>G ENSP00000485570.1:n.166+500A>G
NM_012387.2:c.255T>C NP_036519.2:p.Gly85=
XM_011541150.1:c.255T>C XP_011539452.1:p.Gly85=
XM_011541151.1:c.255T>C XP_011539453.1:p.Gly85=
XM_011541153.1:c.255T>C XP_011539455.1:p.Gly85=
XM_011541154.1:c.255T>C XP_011539456.1:p.Gly85=
XM_011541155.1:c.255T>C XP_011539457.1:p.Gly85=
XM_011541156.1:c.255T>C XP_011539458.1:p.Gly85=
XM_011541154.2:c.255T>C XP_011539456.1:p.Gly85=
NM_012387.3:c.255T>C MANE Select NP_036519.2:p.Gly85=