Canonical Allele Identifier: CA2643694391

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348043-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348044_17348045insTT , CM000663.2:g.17348044_17348045insTT	GRCh38
NC_000001.10:g.17674539_17674540insTT , CM000663.1:g.17674539_17674540insTT	GRCh37
NC_000001.9:g.17547126_17547127insTT	NCBI36
NG_023261.2:g.44855_44856insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.1151_1152insTT MANE Select	ENSP00000364597.4:p.Met385Ter
ENST00000468945.1:n.210_211insTT
ENST00000487048.5:n.118_119insTT
NM_012387.2:c.1151_1152insTT	NP_036519.2:p.Met385Ter
XM_011541150.1:c.965_966insTT	XP_011539452.1:p.Met323Ter
XM_011541151.1:c.1151_1152insTT	XP_011539453.1:p.Met385Ter
XM_011541152.1:c.614_615insTT	XP_011539454.1:p.Met206Ter
XM_011541153.1:c.1151_1152insTT	XP_011539455.1:p.Met385Ter
XM_011541154.1:c.1151_1152insTT	XP_011539456.1:p.Met385Ter
XM_011541155.1:c.1151_1152insTT	XP_011539457.1:p.Met385Ter
XM_011541156.1:c.1151_1152insTT	XP_011539458.1:p.Met385Ter
XM_011541157.1:c.260_261insTT	XP_011539459.1:p.Met88Ter
XM_011541154.2:c.1151_1152insTT	XP_011539456.1:p.Met385Ter
NM_012387.3:c.1151_1152insTT MANE Select	NP_036519.2:p.Met385Ter