Canonical Allele Identifier: CA416403187
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs2100711980
gnomAD v4: 1-17333988-C-T
MyVariant Identifiers: chr1:g.17660483C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17333988C>T , CM000663.2:g.17333988C>T GRCh38
NC_000001.10:g.17660483C>T , CM000663.1:g.17660483C>T GRCh37
NC_000001.9:g.17533070C>T NCBI36
NG_023261.2:g.30799C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.319C>T MANE Select ENSP00000364597.4:p.Leu107=
ENST00000375453.5:c.319C>T ENSP00000364602.1:p.Leu107=
NM_012387.2:c.319C>T NP_036519.2:p.Leu107=
XM_011541150.1:c.319C>T XP_011539452.1:p.Leu107=
XM_011541151.1:c.319C>T XP_011539453.1:p.Leu107=
XM_011541153.1:c.319C>T XP_011539455.1:p.Leu107=
XM_011541154.1:c.319C>T XP_011539456.1:p.Leu107=
XM_011541155.1:c.319C>T XP_011539457.1:p.Leu107=
XM_011541156.1:c.319C>T XP_011539458.1:p.Leu107=
XM_011541157.1:c.-394C>T XP_011539459.1:n.-394C>T
XM_011541154.2:c.319C>T XP_011539456.1:p.Leu107=
NM_012387.3:c.319C>T MANE Select NP_036519.2:p.Leu107=