Canonical Allele Identifier: CA18657082
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs905634568
gnomAD v3: 1-17356164-C-T
gnomAD v4: 1-17356164-C-T
MyVariant Identifiers: chr1:g.17356164C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17356164C>T , CM000663.2:g.17356164C>T GRCh38
NC_000001.10:g.17682659C>T , CM000663.1:g.17682659C>T GRCh37
NC_000001.9:g.17555246C>T NCBI36
NG_023261.2:g.52975C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1455+37C>T MANE Select ENSP00000364597.4:n.1455+37C>T
ENST00000467001.1:n.356+37C>T
ENST00000487048.5:n.422+37C>T
NM_012387.2:c.1455+37C>T NP_036519.2:n.1455+37C>T
XM_011541150.1:c.1269+37C>T XP_011539452.1:n.1269+37C>T
XM_011541151.1:c.1156-193C>T XP_011539453.1:n.1156-193C>T
XM_011541152.1:c.918+37C>T XP_011539454.1:n.918+37C>T
XM_011541157.1:c.564+37C>T XP_011539459.1:n.564+37C>T
NM_012387.3:c.1455+37C>T MANE Select NP_036519.2:n.1455+37C>T