Canonical Allele Identifier: CA1900661196
Gene: NRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.33178497_33178498delinsGT , CM000672.2:g.33178497_33178498delinsGT GRCh38
NC_000010.10:g.33467425_33467426delinsGT , CM000672.1:g.33467425_33467426delinsGT GRCh37
NC_000010.9:g.33507431_33507432delinsGT NCBI36
NG_030328.1:g.161408_161409delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000374867.7:c.*1578_*1579delinsAC MANE Select ENSP00000364001.2:n.*1578_*1579delinsAC
ENST00000265371.8:c.*1578_*1579delinsAC ENSP00000265371.3:n.*1578_*1579delinsAC
ENST00000374867.6:c.*1578_*1579delinsAC ENSP00000364001.2:n.*1578_*1579delinsAC
ENST00000374875.5:c.*1578_*1579delinsAC ENSP00000364009.1:n.*1578_*1579delinsAC
ENST00000395995.5:c.*1578_*1579delinsAC ENSP00000379317.1:n.*1578_*1579delinsAC
NM_001244972.1:c.*1578_*1579delinsAC NP_001231901.1:n.*1578_*1579delinsAC
NM_001244973.1:c.*1578_*1579delinsAC NP_001231902.1:n.*1578_*1579delinsAC
NM_003873.5:c.*1578_*1579delinsAC NP_003864.4:n.*1578_*1579delinsAC
NR_045259.1:n.4670_4671delinsAC
XM_006717521.1:c.*1578_*1579delinsAC XP_006717584.1:n.*1578_*1579delinsAC
XM_006717522.1:c.*1578_*1579delinsAC XP_006717585.1:n.*1578_*1579delinsAC
XM_006717523.1:c.*1578_*1579delinsAC XP_006717586.1:n.*1578_*1579delinsAC
XM_006717524.1:c.*1578_*1579delinsAC XP_006717587.1:n.*1578_*1579delinsAC
XM_006717525.1:c.*1578_*1579delinsAC XP_006717588.1:n.*1578_*1579delinsAC
NM_001330068.1:c.*1578_*1579delinsAC NP_001316997.1:n.*1578_*1579delinsAC
XM_006717521.2:c.*1578_*1579delinsAC XP_006717584.1:n.*1578_*1579delinsAC
XM_006717522.2:c.*1578_*1579delinsAC XP_006717585.1:n.*1578_*1579delinsAC
XM_006717524.2:c.*1578_*1579delinsAC XP_006717587.1:n.*1578_*1579delinsAC
XM_006717525.2:c.*1578_*1579delinsAC XP_006717588.1:n.*1578_*1579delinsAC
XM_017016865.2:c.*1578_*1579delinsAC XP_016872354.1:n.*1578_*1579delinsAC
XM_017016866.2:c.*1578_*1579delinsAC XP_016872355.1:n.*1578_*1579delinsAC
NM_003873.6:c.*1578_*1579delinsAC NP_003864.4:n.*1578_*1579delinsAC
NM_001244972.2:c.*1578_*1579delinsAC NP_001231901.2:n.*1578_*1579delinsAC
NM_001244973.2:c.*1578_*1579delinsAC NP_001231902.2:n.*1578_*1579delinsAC
NM_001330068.2:c.*1578_*1579delinsAC NP_001316997.2:n.*1578_*1579delinsAC
NM_003873.7:c.*1578_*1579delinsAC MANE Select NP_003864.5:n.*1578_*1579delinsAC
NR_045259.2:n.4432_4433delinsAC