Canonical Allele Identifier: CA1156216658
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs2074756619
gnomAD v4: 1-17356166-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17356166T>C , CM000663.2:g.17356166T>C GRCh38
NC_000001.10:g.17682661T>C , CM000663.1:g.17682661T>C GRCh37
NC_000001.9:g.17555248T>C NCBI36
NG_023261.2:g.52977T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1455+39T>C MANE Select ENSP00000364597.4:n.1455+39T>C
ENST00000467001.1:n.356+39T>C
ENST00000487048.5:n.422+39T>C
NM_012387.2:c.1455+39T>C NP_036519.2:n.1455+39T>C
XM_011541150.1:c.1269+39T>C XP_011539452.1:n.1269+39T>C
XM_011541151.1:c.1156-191T>C XP_011539453.1:n.1156-191T>C
XM_011541152.1:c.918+39T>C XP_011539454.1:n.918+39T>C
XM_011541157.1:c.564+39T>C XP_011539459.1:n.564+39T>C
NM_012387.3:c.1455+39T>C MANE Select NP_036519.2:n.1455+39T>C
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