Canonical Allele Identifier: CA2742645092
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348338A>C , CM000663.2:g.17348338A>C GRCh38
NC_000001.10:g.17674833A>C , CM000663.1:g.17674833A>C GRCh37
NC_000001.9:g.17547420A>C NCBI36
NG_023261.2:g.45149A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+290A>C MANE Select ENSP00000364597.4:n.1155+290A>C
ENST00000487048.5:n.122+290A>C
NM_012387.2:c.1155+290A>C NP_036519.2:n.1155+290A>C
XM_011541150.1:c.969+290A>C XP_011539452.1:n.969+290A>C
XM_011541151.1:c.1155+290A>C XP_011539453.1:n.1155+290A>C
XM_011541152.1:c.618+290A>C XP_011539454.1:n.618+290A>C
XM_011541153.1:c.1155+290A>C XP_011539455.1:n.1155+290A>C
XM_011541154.1:c.1155+290A>C XP_011539456.1:n.1155+290A>C
XM_011541155.1:c.1155+290A>C XP_011539457.1:n.1155+290A>C
XM_011541156.1:c.1155+290A>C XP_011539458.1:n.1155+290A>C
XM_011541157.1:c.264+290A>C XP_011539459.1:n.264+290A>C
XM_011541154.2:c.1155+290A>C XP_011539456.1:n.1155+290A>C
NM_012387.3:c.1155+290A>C MANE Select NP_036519.2:n.1155+290A>C