Canonical Allele Identifier: CA883690014

Gene: NLRP7 NCR1

Linked Data

• MyVariant Identifiers: chr19:g.54937920_54937921insAAAAAAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54937921_54937922insAAAAAAATA , CM000681.2:g.54937921_54937922insAAAAAAATA	GRCh38
NC_000019.8:g.60141101_60141102insAAAAAAATA	NCBI36
NG_008056.1:g.14585_14586insATTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592784.6:c.2129+123_2129+124insATTTTTTTT (NLRP7) MANE Select	ENSP00000468706.1:n.2129+123_2129+124insATTTTTTTT
ENST00000328092.9:c.2045+123_2045+124insATTTTTTTT (NLRP7)	ENSP00000329568.5:n.2045+123_2045+124insATTTTTTTT
ENST00000340844.6:c.2129+123_2129+124insATTTTTTTT (NLRP7)	ENSP00000339491.2:n.2129+123_2129+124insATTTTTTTT
ENST00000586379.5:c.2129+123_2129+124insATTTTTTTT (NLRP7)	ENSP00000468243.1:n.2129+123_2129+124insATTTTTTTT
ENST00000588756.5:c.2129+123_2129+124insATTTTTTTT (NLRP7)	ENSP00000467123.1:n.2129+123_2129+124insATTTTTTTT
ENST00000590030.5:c.2129+123_2129+124insATTTTTTTT (NLRP7)	ENSP00000465520.1:n.2129+123_2129+124insATTTTTTTT
ENST00000592784.5:c.2129+123_2129+124insATTTTTTTT (NLRP7)	ENSP00000468706.1:n.2129+123_2129+124insATTTTTTTT
NM_001127255.1:c.2129+123_2129+124insATTTTTTTT (NLRP7)	NP_001120727.1:n.2129+123_2129+124insATTTTTTTT
NM_139176.3:c.2045+123_2045+124insATTTTTTTT (NLRP7)	NP_631915.2:n.2045+123_2045+124insATTTTTTTT
NM_206828.3:c.2129+123_2129+124insATTTTTTTT (NLRP7)	NP_996611.2:n.2129+123_2129+124insATTTTTTTT
XM_006723075.2:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_006723138.1:n.2129+123_2129+124insATTTTTTTT
XM_006723076.2:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_006723139.1:n.2129+123_2129+124insATTTTTTTT
XM_011526596.1:c.2213+123_2213+124insATTTTTTTT (NLRP7)	XP_011524898.1:n.2213+123_2213+124insATTTTTTTT
XM_011526597.1:c.2213+123_2213+124insATTTTTTTT (NLRP7)	XP_011524899.1:n.2213+123_2213+124insATTTTTTTT
XM_011526598.1:c.2213+123_2213+124insATTTTTTTT (NLRP7)	XP_011524900.1:n.2213+123_2213+124insATTTTTTTT
XM_011526599.1:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_011524901.1:n.2129+123_2129+124insATTTTTTTT
XM_011526600.1:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_011524902.1:n.2129+123_2129+124insATTTTTTTT
XM_011526601.1:c.2213+123_2213+124insATTTTTTTT (NLRP7)	XP_011524903.1:n.2213+123_2213+124insATTTTTTTT
XM_011527530.1:c.683-215_683-214insAAAAAAATA (NCR1)	XP_011525832.1:n.683-215_683-214insAAAAAAATA
XR_935761.1:n.2647+123_2647+124insATTTTTTTT (NLRP7)
XM_006723075.3:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_006723138.1:n.2129+123_2129+124insATTTTTTTT
XM_006723076.3:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_006723139.1:n.2129+123_2129+124insATTTTTTTT
XM_011526596.2:c.2213+123_2213+124insATTTTTTTT (NLRP7)	XP_011524898.1:n.2213+123_2213+124insATTTTTTTT
XM_011526599.2:c.2129+123_2129+124insATTTTTTTT (NLRP7)	XP_011524901.1:n.2129+123_2129+124insATTTTTTTT
XM_011526601.2:c.2213+123_2213+124insATTTTTTTT (NLRP7)	XP_011524903.1:n.2213+123_2213+124insATTTTTTTT
XM_011527530.3:c.683-215_683-214insAAAAAAATA (NCR1)	XP_011525832.1:n.683-215_683-214insAAAAAAATA