Canonical Allele Identifier: CA1156099169
Gene: PADI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17117924A= , CM000663.2:g.17117924A= GRCh38
NC_000001.10:g.17444419A= , CM000663.1:g.17444419A= GRCh37
NC_000001.9:g.17317006A= NCBI36
NG_033958.1:g.6530T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1356T= MANE Select ENSP00000364635.4:n.92+1356T=
ENST00000375481.1:c.92+1356T= ENSP00000364630.1:n.92+1356T=
ENST00000375486.8:c.92+1356T= ENSP00000364635.4:n.92+1356T=
NM_007365.2:c.92+1356T= NP_031391.2:n.92+1356T=
XM_011540549.1:c.92+1356T= XP_011538851.1:n.92+1356T=
XR_947004.1:n.4500A=
XR_001736944.1:n.174+1356T=
NM_007365.3:c.92+1356T= MANE Select NP_031391.2:n.92+1356T=