Canonical Allele Identifier: CA407862177
Gene: NLRP7 HGNC NCBI

Linked Data

dbSNP Id: rs1569540576
MyVariant Identifiers: chr19:g.54939468C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54939468C>T , CM000681.2:g.54939468C>T GRCh38
NC_000019.8:g.60142648C>T NCBI36
NG_008056.1:g.13038G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000592784.6:c.1351G>A MANE Select ENSP00000468706.1:p.Gly451Arg
ENST00000328092.9:c.1351G>A ENSP00000329568.5:p.Gly451Arg
ENST00000340844.6:c.1351G>A ENSP00000339491.2:p.Gly451Arg
ENST00000586379.5:c.1351G>A ENSP00000468243.1:p.Gly451Arg
ENST00000588756.5:c.1351G>A ENSP00000467123.1:p.Gly451Arg
ENST00000590030.5:c.1351G>A ENSP00000465520.1:p.Gly451Arg
ENST00000592784.5:c.1351G>A ENSP00000468706.1:p.Gly451Arg
NM_001127255.1:c.1351G>A NP_001120727.1:p.Gly451Arg
NM_139176.3:c.1351G>A NP_631915.2:p.Gly451Arg
NM_206828.3:c.1351G>A NP_996611.2:p.Gly451Arg
XM_006723075.2:c.1351G>A XP_006723138.1:p.Gly451Arg
XM_006723076.2:c.1351G>A XP_006723139.1:p.Gly451Arg
XM_011526596.1:c.1435G>A XP_011524898.1:p.Gly479Arg
XM_011526597.1:c.1435G>A XP_011524899.1:p.Gly479Arg
XM_011526598.1:c.1435G>A XP_011524900.1:p.Gly479Arg
XM_011526599.1:c.1351G>A XP_011524901.1:p.Gly451Arg
XM_011526600.1:c.1351G>A XP_011524902.1:p.Gly451Arg
XM_011526601.1:c.1435G>A XP_011524903.1:p.Gly479Arg
XR_935761.1:n.1869G>A
XM_006723075.3:c.1351G>A XP_006723138.1:p.Gly451Arg
XM_006723076.3:c.1351G>A XP_006723139.1:p.Gly451Arg
XM_011526596.2:c.1435G>A XP_011524898.1:p.Gly479Arg
XM_011526599.2:c.1351G>A XP_011524901.1:p.Gly451Arg
XM_011526601.2:c.1435G>A XP_011524903.1:p.Gly479Arg