Canonical Allele Identifier: CA2342535114
Gene: NLRP12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53807610A= , CM000681.2:g.53807610A= GRCh38
NC_000019.9:g.54310864A= , CM000681.1:g.54310864A= GRCh37
NC_000019.8:g.59002676A= NCBI36
NG_008651.1:g.21785T=
NG_008651.2:g.21785T=

Transcript Alleles

HGVS Amino-acid change
ENST00000391773.7:c.2131T= ENSP00000375653.1:p.Cys711=
ENST00000324134.11:c.2128T= MANE Select ENSP00000319377.6:p.Cys710=
ENST00000391773.6:c.2131T= ENSP00000375653.1:p.Cys711=
ENST00000324134.10:c.2128T= ENSP00000319377.6:p.Cys710=
ENST00000345770.9:c.2131T= ENSP00000341428.5:p.Cys711=
ENST00000391772.1:c.2131T= ENSP00000375652.1:p.Cys711=
ENST00000391773.5:c.2131T= ENSP00000375653.1:p.Cys711=
ENST00000391775.7:c.2128T= ENSP00000375655.3:p.Cys710=
ENST00000492915.1:n.1096T=
NM_001277126.1:c.2131T= NP_001264055.1:p.Cys711=
NM_001277129.1:c.2128T= NP_001264058.1:p.Cys710=
NM_144687.3:c.2128T= NP_653288.1:p.Cys710=
XM_011527478.1:c.1963T= XP_011525780.1:p.Cys655=
XM_011527479.1:c.2131T= XP_011525781.1:p.Cys711=
XM_011527480.1:c.2131T= XP_011525782.1:p.Cys711=
XM_011527481.1:c.2131T= XP_011525783.1:p.Cys711=
XM_011527482.1:c.2131T= XP_011525784.1:p.Cys711=
XM_011527483.1:c.2072+1977T= XP_011525785.1:n.2072+1977T=
XM_017027460.1:c.2131T= XP_016882949.1:p.Cys711=
XM_017027461.1:c.2131T= XP_016882950.1:p.Cys711=
XM_017027462.1:c.2072+1977T= XP_016882951.1:n.2072+1977T=
XM_017027463.1:c.1714T= XP_016882952.1:p.Cys572=
XM_017027464.1:c.1714T= XP_016882953.1:p.Cys572=
XM_017027465.1:c.1714T= XP_016882954.1:p.Cys572=
XM_017027466.1:c.1714T= XP_016882955.1:p.Cys572=
XM_017027467.1:c.1714T= XP_016882956.1:p.Cys572=
NM_001277126.2:c.2131T= NP_001264055.1:p.Cys711=
NM_144687.4:c.2128T= MANE Select NP_653288.1:p.Cys710=