Canonical Allele Identifier: CA592499877

Gene: NRP1

Linked Data

• dbSNP Id: rs397945276
• gnomAD v2: 10-33467414-T-TC
• gnomAD v3: 10-33178486-T-TC
• gnomAD v4: 10-33178486-T-TC
• MyVariant Identifiers: chr10:g.33467414_33467415insC (hg19) ; chr10:g.33178486_33178487insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.33178486_33178487insC , CM000672.2:g.33178486_33178487insC	GRCh38
NC_000010.10:g.33467414_33467415insC , CM000672.1:g.33467414_33467415insC	GRCh37
NC_000010.9:g.33507420_33507421insC	NCBI36
NG_030328.1:g.161419_161420insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374867.7:c.*1589_*1590insG MANE Select	ENSP00000364001.2:n.*1589_*1590insG
ENST00000265371.8:c.*1589_*1590insG	ENSP00000265371.3:n.*1589_*1590insG
ENST00000374867.6:c.*1589_*1590insG	ENSP00000364001.2:n.*1589_*1590insG
ENST00000374875.5:c.*1589_*1590insG	ENSP00000364009.1:n.*1589_*1590insG
ENST00000395995.5:c.*1589_*1590insG	ENSP00000379317.1:n.*1589_*1590insG
NM_001244972.1:c.*1589_*1590insG	NP_001231901.1:n.*1589_*1590insG
NM_001244973.1:c.*1589_*1590insG	NP_001231902.1:n.*1589_*1590insG
NM_003873.5:c.*1589_*1590insG	NP_003864.4:n.*1589_*1590insG
NR_045259.1:n.4681_4682insG
XM_006717521.1:c.*1589_*1590insG	XP_006717584.1:n.*1589_*1590insG
XM_006717522.1:c.*1589_*1590insG	XP_006717585.1:n.*1589_*1590insG
XM_006717523.1:c.*1589_*1590insG	XP_006717586.1:n.*1589_*1590insG
XM_006717524.1:c.*1589_*1590insG	XP_006717587.1:n.*1589_*1590insG
XM_006717525.1:c.*1589_*1590insG	XP_006717588.1:n.*1589_*1590insG
NM_001330068.1:c.*1589_*1590insG	NP_001316997.1:n.*1589_*1590insG
XM_006717521.2:c.*1589_*1590insG	XP_006717584.1:n.*1589_*1590insG
XM_006717522.2:c.*1589_*1590insG	XP_006717585.1:n.*1589_*1590insG
XM_006717524.2:c.*1589_*1590insG	XP_006717587.1:n.*1589_*1590insG
XM_006717525.2:c.*1589_*1590insG	XP_006717588.1:n.*1589_*1590insG
XM_017016865.2:c.*1589_*1590insG	XP_016872354.1:n.*1589_*1590insG
XM_017016866.2:c.*1589_*1590insG	XP_016872355.1:n.*1589_*1590insG
NM_003873.6:c.*1589_*1590insG	NP_003864.4:n.*1589_*1590insG
NM_001244972.2:c.*1589_*1590insG	NP_001231901.2:n.*1589_*1590insG
NM_001244973.2:c.*1589_*1590insG	NP_001231902.2:n.*1589_*1590insG
NM_001330068.2:c.*1589_*1590insG	NP_001316997.2:n.*1589_*1590insG
NM_003873.7:c.*1589_*1590insG MANE Select	NP_003864.5:n.*1589_*1590insG
NR_045259.2:n.4443_4444insG