Canonical Allele Identifier: CA2721111249

Gene: NRP1

Linked Data

• dbSNP Id: rs34299487

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.33178486del , CM000672.2:g.33178486del	GRCh38
NC_000010.10:g.33467414del , CM000672.1:g.33467414del	GRCh37
NC_000010.9:g.33507420del	NCBI36
NG_030328.1:g.161422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374867.7:c.*1592del MANE Select	ENSP00000364001.2:n.*1592del
ENST00000265371.8:c.*1592del	ENSP00000265371.3:n.*1592del
ENST00000374867.6:c.*1592del	ENSP00000364001.2:n.*1592del
ENST00000374875.5:c.*1592del	ENSP00000364009.1:n.*1592del
ENST00000395995.5:c.*1592del	ENSP00000379317.1:n.*1592del
NM_001244972.1:c.*1592del	NP_001231901.1:n.*1592del
NM_001244973.1:c.*1592del	NP_001231902.1:n.*1592del
NM_003873.5:c.*1592del	NP_003864.4:n.*1592del
NR_045259.1:n.4684del
XM_006717521.1:c.*1592del	XP_006717584.1:n.*1592del
XM_006717522.1:c.*1592del	XP_006717585.1:n.*1592del
XM_006717523.1:c.*1592del	XP_006717586.1:n.*1592del
XM_006717524.1:c.*1592del	XP_006717587.1:n.*1592del
XM_006717525.1:c.*1592del	XP_006717588.1:n.*1592del
NM_001330068.1:c.*1592del	NP_001316997.1:n.*1592del
XM_006717521.2:c.*1592del	XP_006717584.1:n.*1592del
XM_006717522.2:c.*1592del	XP_006717585.1:n.*1592del
XM_006717524.2:c.*1592del	XP_006717587.1:n.*1592del
XM_006717525.2:c.*1592del	XP_006717588.1:n.*1592del
XM_017016865.2:c.*1592del	XP_016872354.1:n.*1592del
XM_017016866.2:c.*1592del	XP_016872355.1:n.*1592del
NM_003873.6:c.*1592del	NP_003864.4:n.*1592del
NM_001244972.2:c.*1592del	NP_001231901.2:n.*1592del
NM_001244973.2:c.*1592del	NP_001231902.2:n.*1592del
NM_001330068.2:c.*1592del	NP_001316997.2:n.*1592del
NM_003873.7:c.*1592del MANE Select	NP_003864.5:n.*1592del
NR_045259.2:n.4446del