Canonical Allele Identifier: CA376476901

Gene: NRP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374867.7:c.2197G>T MANE Select	ENSP00000364001.2:p.Val733Phe
ENST00000265371.8:c.2197G>T	ENSP00000265371.3:p.Val733Phe
ENST00000374867.6:c.2197G>T	ENSP00000364001.2:p.Val733Phe
ENST00000374875.5:c.1633G>T	ENSP00000364009.1:p.Val545Phe
ENST00000395995.5:c.2197G>T	ENSP00000379317.1:p.Val733Phe
NM_001244972.1:c.2179G>T	NP_001231901.1:p.Val727Phe
NM_001244973.1:c.2176G>T	NP_001231902.1:p.Val726Phe
NM_003873.5:c.2197G>T	NP_003864.4:p.Val733Phe
NR_045259.1:n.2517G>T
XM_006717521.1:c.2200G>T	XP_006717584.1:p.Val734Phe
XM_006717522.1:c.2200G>T	XP_006717585.1:p.Val734Phe
XM_006717523.1:c.2197G>T	XP_006717586.1:p.Val733Phe
XM_006717524.1:c.2095G>T	XP_006717587.1:p.Val699Phe
XM_006717525.1:c.2092G>T	XP_006717588.1:p.Val698Phe
NM_001330068.1:c.2197G>T	NP_001316997.1:p.Val733Phe
XM_006717521.2:c.2200G>T	XP_006717584.1:p.Val734Phe
XM_006717522.2:c.2200G>T	XP_006717585.1:p.Val734Phe
XM_006717524.2:c.2095G>T	XP_006717587.1:p.Val699Phe
XM_006717525.2:c.2092G>T	XP_006717588.1:p.Val698Phe
XM_017016865.2:c.2176G>T	XP_016872354.1:p.Val726Phe
XM_017016866.2:c.1654G>T	XP_016872355.1:p.Val552Phe
NM_003873.6:c.2197G>T	NP_003864.4:p.Val733Phe
NM_001244972.2:c.2179G>T	NP_001231901.2:p.Val727Phe
NM_001244973.2:c.2176G>T	NP_001231902.2:p.Val726Phe
NM_001330068.2:c.2197G>T	NP_001316997.2:p.Val733Phe
NM_003873.7:c.2197G>T MANE Select	NP_003864.5:p.Val733Phe
NR_045259.2:n.2279G>T