Canonical Allele Identifier: CA592499843

Gene: NRP1

Linked Data

• dbSNP Id: rs1269643465
• gnomAD v2: 10-33467151-G-T
• gnomAD v3: 10-33178223-G-T
• gnomAD v4: 10-33178223-G-T
• MyVariant Identifiers: chr10:g.33467151G>T (hg19) ; chr10:g.33178223G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.33178223G>T , CM000672.2:g.33178223G>T	GRCh38
NC_000010.10:g.33467151G>T , CM000672.1:g.33467151G>T	GRCh37
NC_000010.9:g.33507157G>T	NCBI36
NG_030328.1:g.161683C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374867.7:c.*1853C>A MANE Select	ENSP00000364001.2:n.*1853C>A
ENST00000265371.8:c.*1853C>A	ENSP00000265371.3:n.*1853C>A
ENST00000374867.6:c.*1853C>A	ENSP00000364001.2:n.*1853C>A
ENST00000374875.5:c.*1853C>A	ENSP00000364009.1:n.*1853C>A
ENST00000395995.5:c.*1853C>A	ENSP00000379317.1:n.*1853C>A
NM_001244972.1:c.*1853C>A	NP_001231901.1:n.*1853C>A
NM_001244973.1:c.*1853C>A	NP_001231902.1:n.*1853C>A
NM_003873.5:c.*1853C>A	NP_003864.4:n.*1853C>A
NR_045259.1:n.4945C>A
XM_006717521.1:c.*1853C>A	XP_006717584.1:n.*1853C>A
XM_006717522.1:c.*1853C>A	XP_006717585.1:n.*1853C>A
XM_006717523.1:c.*1853C>A	XP_006717586.1:n.*1853C>A
XM_006717524.1:c.*1853C>A	XP_006717587.1:n.*1853C>A
XM_006717525.1:c.*1853C>A	XP_006717588.1:n.*1853C>A
NM_001330068.1:c.*1853C>A	NP_001316997.1:n.*1853C>A
XM_006717521.2:c.*1853C>A	XP_006717584.1:n.*1853C>A
XM_006717522.2:c.*1853C>A	XP_006717585.1:n.*1853C>A
XM_006717524.2:c.*1853C>A	XP_006717587.1:n.*1853C>A
XM_006717525.2:c.*1853C>A	XP_006717588.1:n.*1853C>A
XM_017016865.2:c.*1853C>A	XP_016872354.1:n.*1853C>A
XM_017016866.2:c.*1853C>A	XP_016872355.1:n.*1853C>A
NM_003873.6:c.*1853C>A	NP_003864.4:n.*1853C>A
NM_001244972.2:c.*1853C>A	NP_001231901.2:n.*1853C>A
NM_001244973.2:c.*1853C>A	NP_001231902.2:n.*1853C>A
NM_001330068.2:c.*1853C>A	NP_001316997.2:n.*1853C>A
NM_003873.7:c.*1853C>A MANE Select	NP_003864.5:n.*1853C>A
NR_045259.2:n.4707C>A