Canonical Allele Identifier: CA407415653

Gene: NLRP12

Linked Data

• MyVariant Identifiers: chr19:g.54314057G>T (hg19) ; chr19:g.53810803G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53810803G>T , CM000681.2:g.53810803G>T	GRCh38
NC_000019.9:g.54314057G>T , CM000681.1:g.54314057G>T	GRCh37
NC_000019.8:g.59005869G>T	NCBI36
NG_008651.1:g.18592C>A
NG_008651.2:g.18592C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000391773.7:c.856C>A	ENSP00000375653.1:p.Pro286Thr
ENST00000324134.11:c.856C>A MANE Select	ENSP00000319377.6:p.Pro286Thr
ENST00000391773.6:c.856C>A	ENSP00000375653.1:p.Pro286Thr
ENST00000324134.10:c.856C>A	ENSP00000319377.6:p.Pro286Thr
ENST00000345770.9:c.856C>A	ENSP00000341428.5:p.Pro286Thr
ENST00000391772.1:c.856C>A	ENSP00000375652.1:p.Pro286Thr
ENST00000391773.5:c.856C>A	ENSP00000375653.1:p.Pro286Thr
ENST00000391775.7:c.856C>A	ENSP00000375655.3:p.Pro286Thr
NM_001277126.1:c.856C>A	NP_001264055.1:p.Pro286Thr
NM_001277129.1:c.856C>A	NP_001264058.1:p.Pro286Thr
NM_144687.3:c.856C>A	NP_653288.1:p.Pro286Thr
XM_011527478.1:c.688C>A	XP_011525780.1:p.Pro230Thr
XM_011527479.1:c.856C>A	XP_011525781.1:p.Pro286Thr
XM_011527480.1:c.856C>A	XP_011525782.1:p.Pro286Thr
XM_011527481.1:c.856C>A	XP_011525783.1:p.Pro286Thr
XM_011527482.1:c.856C>A	XP_011525784.1:p.Pro286Thr
XM_011527483.1:c.856C>A	XP_011525785.1:p.Pro286Thr
XM_017027460.1:c.856C>A	XP_016882949.1:p.Pro286Thr
XM_017027461.1:c.856C>A	XP_016882950.1:p.Pro286Thr
XM_017027462.1:c.856C>A	XP_016882951.1:p.Pro286Thr
XM_017027463.1:c.439C>A	XP_016882952.1:p.Pro147Thr
XM_017027464.1:c.439C>A	XP_016882953.1:p.Pro147Thr
XM_017027465.1:c.439C>A	XP_016882954.1:p.Pro147Thr
XM_017027466.1:c.439C>A	XP_016882955.1:p.Pro147Thr
XM_017027467.1:c.439C>A	XP_016882956.1:p.Pro147Thr
NM_001277126.2:c.856C>A	NP_001264055.1:p.Pro286Thr
NM_144687.4:c.856C>A MANE Select	NP_653288.1:p.Pro286Thr