Canonical Allele Identifier: CA2343150160

Gene: NLRP7 NCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54938096G= , CM000681.2:g.54938096G=	GRCh38
NC_000019.8:g.60141276G=	NCBI36
NG_008056.1:g.14410C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592784.6:c.2077C= (NLRP7) MANE Select	ENSP00000468706.1:p.Arg693=
ENST00000328092.9:c.1993C= (NLRP7)	ENSP00000329568.5:p.Arg665=
ENST00000340844.6:c.2077C= (NLRP7)	ENSP00000339491.2:p.Arg693=
ENST00000586379.5:c.2077C= (NLRP7)	ENSP00000468243.1:p.Arg693=
ENST00000588756.5:c.2077C= (NLRP7)	ENSP00000467123.1:p.Arg693=
ENST00000590030.5:c.2077C= (NLRP7)	ENSP00000465520.1:p.Arg693=
ENST00000592784.5:c.2077C= (NLRP7)	ENSP00000468706.1:p.Arg693=
NM_001127255.1:c.2077C= (NLRP7)	NP_001120727.1:p.Arg693=
NM_139176.3:c.1993C= (NLRP7)	NP_631915.2:p.Arg665=
NM_206828.3:c.2077C= (NLRP7)	NP_996611.2:p.Arg693=
XM_006723075.2:c.2077C= (NLRP7)	XP_006723138.1:p.Arg693=
XM_006723076.2:c.2077C= (NLRP7)	XP_006723139.1:p.Arg693=
XM_011526596.1:c.2161C= (NLRP7)	XP_011524898.1:p.Arg721=
XM_011526597.1:c.2161C= (NLRP7)	XP_011524899.1:p.Arg721=
XM_011526598.1:c.2161C= (NLRP7)	XP_011524900.1:p.Arg721=
XM_011526599.1:c.2077C= (NLRP7)	XP_011524901.1:p.Arg693=
XM_011526600.1:c.2077C= (NLRP7)	XP_011524902.1:p.Arg693=
XM_011526601.1:c.2161C= (NLRP7)	XP_011524903.1:p.Arg721=
XM_011527530.1:c.683-40G= (NCR1)	XP_011525832.1:n.683-40G=
XR_935761.1:n.2595C= (NLRP7)
XM_006723075.3:c.2077C= (NLRP7)	XP_006723138.1:p.Arg693=
XM_006723076.3:c.2077C= (NLRP7)	XP_006723139.1:p.Arg693=
XM_011526596.2:c.2161C= (NLRP7)	XP_011524898.1:p.Arg721=
XM_011526599.2:c.2077C= (NLRP7)	XP_011524901.1:p.Arg693=
XM_011526601.2:c.2161C= (NLRP7)	XP_011524903.1:p.Arg721=
XM_011527530.3:c.683-40G= (NCR1)	XP_011525832.1:n.683-40G=