Canonical Allele Identifier: CA416412234
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17674540G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348045G>C , CM000663.2:g.17348045G>C GRCh38
NC_000001.10:g.17674540G>C , CM000663.1:g.17674540G>C GRCh37
NC_000001.9:g.17547127G>C NCBI36
NG_023261.2:g.44856G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1152G>C MANE Select ENSP00000364597.4:p.Val384=
ENST00000468945.1:n.211G>C
ENST00000487048.5:n.119G>C
NM_012387.2:c.1152G>C NP_036519.2:p.Val384=
XM_011541150.1:c.966G>C XP_011539452.1:p.Val322=
XM_011541151.1:c.1152G>C XP_011539453.1:p.Val384=
XM_011541152.1:c.615G>C XP_011539454.1:p.Val205=
XM_011541153.1:c.1152G>C XP_011539455.1:p.Val384=
XM_011541154.1:c.1152G>C XP_011539456.1:p.Val384=
XM_011541155.1:c.1152G>C XP_011539457.1:p.Val384=
XM_011541156.1:c.1152G>C XP_011539458.1:p.Val384=
XM_011541157.1:c.261G>C XP_011539459.1:p.Val87=
XM_011541154.2:c.1152G>C XP_011539456.1:p.Val384=
NM_012387.3:c.1152G>C MANE Select NP_036519.2:p.Val384=