Canonical Allele Identifier: CA310068001
Gene: NLRP12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53808703A>C , CM000681.2:g.53808703A>C GRCh38
NC_000019.9:g.54311957A>C , CM000681.1:g.54311957A>C GRCh37
NC_000019.8:g.59003769A>C NCBI36
NG_008651.1:g.20692T>G
NG_008651.2:g.20692T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000391773.7:c.2072+884T>G ENSP00000375653.1:n.2072+884T>G
ENST00000324134.11:c.2072+884T>G MANE Select ENSP00000319377.6:n.2072+884T>G
ENST00000391773.6:c.2072+884T>G ENSP00000375653.1:n.2072+884T>G
ENST00000324134.10:c.2072+884T>G ENSP00000319377.6:n.2072+884T>G
ENST00000345770.9:c.2072+884T>G ENSP00000341428.5:n.2072+884T>G
ENST00000391772.1:c.2072+884T>G ENSP00000375652.1:n.2072+884T>G
ENST00000391773.5:c.2072+884T>G ENSP00000375653.1:n.2072+884T>G
ENST00000391775.7:c.2072+884T>G ENSP00000375655.3:n.2072+884T>G
ENST00000492915.1:n.3T>G
NM_001277126.1:c.2072+884T>G NP_001264055.1:n.2072+884T>G
NM_001277129.1:c.2072+884T>G NP_001264058.1:n.2072+884T>G
NM_144687.3:c.2072+884T>G NP_653288.1:n.2072+884T>G
XM_011527478.1:c.1904+884T>G XP_011525780.1:n.1904+884T>G
XM_011527479.1:c.2072+884T>G XP_011525781.1:n.2072+884T>G
XM_011527480.1:c.2072+884T>G XP_011525782.1:n.2072+884T>G
XM_011527481.1:c.2072+884T>G XP_011525783.1:n.2072+884T>G
XM_011527482.1:c.2072+884T>G XP_011525784.1:n.2072+884T>G
XM_011527483.1:c.2072+884T>G XP_011525785.1:n.2072+884T>G
XM_017027460.1:c.2072+884T>G XP_016882949.1:n.2072+884T>G
XM_017027461.1:c.2072+884T>G XP_016882950.1:n.2072+884T>G
XM_017027462.1:c.2072+884T>G XP_016882951.1:n.2072+884T>G
XM_017027463.1:c.1655+884T>G XP_016882952.1:n.1655+884T>G
XM_017027464.1:c.1655+884T>G XP_016882953.1:n.1655+884T>G
XM_017027465.1:c.1655+884T>G XP_016882954.1:n.1655+884T>G
XM_017027466.1:c.1655+884T>G XP_016882955.1:n.1655+884T>G
XM_017027467.1:c.1655+884T>G XP_016882956.1:n.1655+884T>G
NM_001277126.2:c.2072+884T>G NP_001264055.1:n.2072+884T>G
NM_144687.4:c.2072+884T>G MANE Select NP_653288.1:n.2072+884T>G
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