Canonical Allele Identifier: CA2343151685

Gene: NLRP7

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54940930C= , CM000681.2:g.54940930C=	GRCh38
NC_000019.8:g.60144110C=	NCBI36
NG_008056.1:g.11576G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592784.6:c.352+1G= MANE Select	ENSP00000468706.1:n.352+1G=
NM_001127255.1:c.352+1G=	NP_001120727.1:n.352+1G=
NM_139176.3:c.352+1G=	NP_631915.2:n.352+1G=
NM_206828.3:c.352+1G=	NP_996611.2:n.352+1G=
ENST00000328092.9:c.352+1G=	ENSP00000329568.5:n.352+1G=
ENST00000340844.6:c.352+1G=	ENSP00000339491.2:n.352+1G=
ENST00000586379.5:c.352+1G=	ENSP00000468243.1:n.352+1G=
ENST00000588756.5:c.352+1G=	ENSP00000467123.1:n.352+1G=
ENST00000590030.5:c.352+1G=	ENSP00000465520.1:n.352+1G=
ENST00000592784.5:c.352+1G=	ENSP00000468706.1:n.352+1G=
XM_006723075.2:c.352+1G=	XP_006723138.1:n.352+1G=
XM_006723075.3:c.352+1G=	XP_006723138.1:n.352+1G=
XM_006723076.2:c.352+1G=	XP_006723139.1:n.352+1G=
XM_006723076.3:c.352+1G=	XP_006723139.1:n.352+1G=
XM_011526596.1:c.436+1G=	XP_011524898.1:n.436+1G=
XM_011526596.2:c.436+1G=	XP_011524898.1:n.436+1G=
XM_011526597.1:c.436+1G=	XP_011524899.1:n.436+1G=
XM_011526598.1:c.436+1G=	XP_011524900.1:n.436+1G=
XM_011526599.1:c.352+1G=	XP_011524901.1:n.352+1G=
XM_011526599.2:c.352+1G=	XP_011524901.1:n.352+1G=
XM_011526600.1:c.352+1G=	XP_011524902.1:n.352+1G=
XM_011526601.1:c.436+1G=	XP_011524903.1:n.436+1G=
XM_011526601.2:c.436+1G=	XP_011524903.1:n.436+1G=
XR_935761.1:n.870+1G=