Canonical Allele Identifier: CA416403311

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17660503G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334008G>C , CM000663.2:g.17334008G>C	GRCh38
NC_000001.10:g.17660503G>C , CM000663.1:g.17660503G>C	GRCh37
NC_000001.9:g.17533090G>C	NCBI36
NG_023261.2:g.30819G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.339G>C MANE Select	ENSP00000364597.4:p.Val113=
ENST00000375453.5:c.339G>C	ENSP00000364602.1:p.Val113=
NM_012387.2:c.339G>C	NP_036519.2:p.Val113=
XM_011541150.1:c.339G>C	XP_011539452.1:p.Val113=
XM_011541151.1:c.339G>C	XP_011539453.1:p.Val113=
XM_011541152.1:c.-81G>C	XP_011539454.1:n.-81G>C
XM_011541153.1:c.339G>C	XP_011539455.1:p.Val113=
XM_011541154.1:c.339G>C	XP_011539456.1:p.Val113=
XM_011541155.1:c.339G>C	XP_011539457.1:p.Val113=
XM_011541156.1:c.339G>C	XP_011539458.1:p.Val113=
XM_011541157.1:c.-374G>C	XP_011539459.1:n.-374G>C
XM_011541154.2:c.339G>C	XP_011539456.1:p.Val113=
NM_012387.3:c.339G>C MANE Select	NP_036519.2:p.Val113=