Canonical Allele Identifier: CA640895
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs768467439
gnomAD v2: 1-17682666-G-C
gnomAD v4: 1-17356171-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17356171G>C , CM000663.2:g.17356171G>C GRCh38
NC_000001.10:g.17682666G>C , CM000663.1:g.17682666G>C GRCh37
NC_000001.9:g.17555253G>C NCBI36
NG_023261.2:g.52982G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.1455+44G>C MANE Select ENSP00000364597.4:n.1455+44G>C
ENST00000467001.1:n.356+44G>C
ENST00000487048.5:n.422+44G>C
NM_012387.2:c.1455+44G>C NP_036519.2:n.1455+44G>C
XM_011541150.1:c.1269+44G>C XP_011539452.1:n.1269+44G>C
XM_011541151.1:c.1156-186G>C XP_011539453.1:n.1156-186G>C
XM_011541152.1:c.918+44G>C XP_011539454.1:n.918+44G>C
XM_011541157.1:c.564+44G>C XP_011539459.1:n.564+44G>C
NM_012387.3:c.1455+44G>C MANE Select NP_036519.2:n.1455+44G>C