Canonical Allele Identifier: CA2574237788

Gene: PADI4

Linked Data

• gnomAD v4: 1-17345961-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17345961T>C , CM000663.2:g.17345961T>C	GRCh38
NC_000001.10:g.17672456T>C , CM000663.1:g.17672456T>C	GRCh37
NC_000001.9:g.17545043T>C	NCBI36
NG_023261.2:g.42772T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.936-67T>C MANE Select	ENSP00000364597.4:n.936-67T>C
NM_012387.2:c.936-67T>C	NP_036519.2:n.936-67T>C
XM_011541150.1:c.750-67T>C	XP_011539452.1:n.750-67T>C
XM_011541151.1:c.936-67T>C	XP_011539453.1:n.936-67T>C
XM_011541152.1:c.399-67T>C	XP_011539454.1:n.399-67T>C
XM_011541153.1:c.936-67T>C	XP_011539455.1:n.936-67T>C
XM_011541154.1:c.936-67T>C	XP_011539456.1:n.936-67T>C
XM_011541155.1:c.936-67T>C	XP_011539457.1:n.936-67T>C
XM_011541156.1:c.936-67T>C	XP_011539458.1:n.936-67T>C
XM_011541157.1:c.45-67T>C	XP_011539459.1:n.45-67T>C
XM_011541154.2:c.936-67T>C	XP_011539456.1:n.936-67T>C
NM_012387.3:c.936-67T>C MANE Select	NP_036519.2:n.936-67T>C