Canonical Allele Identifier: CA1900664587

Gene: NRP1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.33186354C= , CM000672.2:g.33186354C=	GRCh38
NC_000010.10:g.33475282C= , CM000672.1:g.33475282C=	GRCh37
NC_000010.9:g.33515288C=	NCBI36
NG_030328.1:g.153552G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003873.7:c.2197G= MANE Select	NP_003864.5:p.Val733=
ENST00000374867.7:c.2197G= MANE Select	ENSP00000364001.2:p.Val733=
NM_001244972.1:c.2179G=	NP_001231901.1:p.Val727=
NM_001244972.2:c.2179G=	NP_001231901.2:p.Val727=
NM_001244973.1:c.2176G=	NP_001231902.1:p.Val726=
NM_001244973.2:c.2176G=	NP_001231902.2:p.Val726=
NM_001330068.1:c.2197G=	NP_001316997.1:p.Val733=
NM_001330068.2:c.2197G=	NP_001316997.2:p.Val733=
NM_003873.5:c.2197G=	NP_003864.4:p.Val733=
NM_003873.6:c.2197G=	NP_003864.4:p.Val733=
NR_045259.1:n.2517G=
NR_045259.2:n.2279G=
ENST00000265371.8:c.2197G=	ENSP00000265371.3:p.Val733=
ENST00000374867.6:c.2197G=	ENSP00000364001.2:p.Val733=
ENST00000374875.5:c.1633G=	ENSP00000364009.1:p.Val545=
ENST00000395995.5:c.2197G=	ENSP00000379317.1:p.Val733=
XM_006717521.1:c.2200G=	XP_006717584.1:p.Val734=
XM_006717521.2:c.2200G=	XP_006717584.1:p.Val734=
XM_006717522.1:c.2200G=	XP_006717585.1:p.Val734=
XM_006717522.2:c.2200G=	XP_006717585.1:p.Val734=
XM_006717523.1:c.2197G=	XP_006717586.1:p.Val733=
XM_006717524.1:c.2095G=	XP_006717587.1:p.Val699=
XM_006717524.2:c.2095G=	XP_006717587.1:p.Val699=
XM_006717525.1:c.2092G=	XP_006717588.1:p.Val698=
XM_006717525.2:c.2092G=	XP_006717588.1:p.Val698=
XM_017016865.2:c.2176G=	XP_016872354.1:p.Val726=
XM_017016866.2:c.1654G=	XP_016872355.1:p.Val552=