Canonical Allele Identifier: CA2342535171

Gene: NLRP12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53807707G= , CM000681.2:g.53807707G=	GRCh38
NC_000019.9:g.54310961G= , CM000681.1:g.54310961G=	GRCh37
NC_000019.8:g.59002773G=	NCBI36
NG_008651.1:g.21688C=
NG_008651.2:g.21688C=

Transcript Alleles

HGVS	Amino-acid Change
NM_144687.4:c.2073-42C= MANE Select	NP_653288.1:n.2073-42C=
ENST00000324134.11:c.2073-42C= MANE Select	ENSP00000319377.6:n.2073-42C=
NM_001277126.1:c.2073-39C=	NP_001264055.1:n.2073-39C=
NM_001277126.2:c.2073-39C=	NP_001264055.1:n.2073-39C=
NM_001277129.1:c.2073-42C=	NP_001264058.1:n.2073-42C=
NM_144687.3:c.2073-42C=	NP_653288.1:n.2073-42C=
ENST00000324134.10:c.2073-42C=	ENSP00000319377.6:n.2073-42C=
ENST00000345770.9:c.2073-39C=	ENSP00000341428.5:n.2073-39C=
ENST00000391772.1:c.2073-39C=	ENSP00000375652.1:n.2073-39C=
ENST00000391773.5:c.2073-39C=	ENSP00000375653.1:n.2073-39C=
ENST00000391773.6:c.2073-39C=	ENSP00000375653.1:n.2073-39C=
ENST00000391773.7:c.2073-39C=	ENSP00000375653.1:n.2073-39C=
ENST00000391775.7:c.2073-42C=	ENSP00000375655.3:n.2073-42C=
ENST00000492915.1:n.999C=
XM_011527478.1:c.1905-39C=	XP_011525780.1:n.1905-39C=
XM_011527479.1:c.2073-39C=	XP_011525781.1:n.2073-39C=
XM_011527480.1:c.2073-39C=	XP_011525782.1:n.2073-39C=
XM_011527481.1:c.2073-39C=	XP_011525783.1:n.2073-39C=
XM_011527482.1:c.2073-39C=	XP_011525784.1:n.2073-39C=
XM_011527483.1:c.2072+1880C=	XP_011525785.1:n.2072+1880C=
XM_017027460.1:c.2073-39C=	XP_016882949.1:n.2073-39C=
XM_017027461.1:c.2073-39C=	XP_016882950.1:n.2073-39C=
XM_017027462.1:c.2072+1880C=	XP_016882951.1:n.2072+1880C=
XM_017027463.1:c.1656-39C=	XP_016882952.1:n.1656-39C=
XM_017027464.1:c.1656-39C=	XP_016882953.1:n.1656-39C=
XM_017027465.1:c.1656-39C=	XP_016882954.1:n.1656-39C=
XM_017027466.1:c.1656-39C=	XP_016882955.1:n.1656-39C=
XM_017027467.1:c.1656-39C=	XP_016882956.1:n.1656-39C=