Canonical Allele Identifier: CA205459300

Gene: NRP1

Linked Data

• dbSNP Id: rs150712214
• gnomAD v2: 10-33466949-C-G
• gnomAD v3: 10-33178021-C-G
• gnomAD v4: 10-33178021-C-G
• MyVariant Identifiers: chr10:g.33466949C>G (hg19) ; chr10:g.33178021C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.33178021C>G , CM000672.2:g.33178021C>G	GRCh38
NC_000010.10:g.33466949C>G , CM000672.1:g.33466949C>G	GRCh37
NC_000010.9:g.33506955C>G	NCBI36
NG_030328.1:g.161885G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374867.7:c.*2055G>C MANE Select	ENSP00000364001.2:n.*2055G>C
ENST00000265371.8:c.*2055G>C	ENSP00000265371.3:n.*2055G>C
ENST00000374867.6:c.*2055G>C	ENSP00000364001.2:n.*2055G>C
ENST00000374875.5:c.*2055G>C	ENSP00000364009.1:n.*2055G>C
ENST00000395995.5:c.*2055G>C	ENSP00000379317.1:n.*2055G>C
NM_001244972.1:c.*2055G>C	NP_001231901.1:n.*2055G>C
NM_001244973.1:c.*2055G>C	NP_001231902.1:n.*2055G>C
NM_003873.5:c.*2055G>C	NP_003864.4:n.*2055G>C
NR_045259.1:n.5147G>C
XM_006717521.1:c.*2055G>C	XP_006717584.1:n.*2055G>C
XM_006717522.1:c.*2055G>C	XP_006717585.1:n.*2055G>C
XM_006717523.1:c.*2055G>C	XP_006717586.1:n.*2055G>C
XM_006717524.1:c.*2055G>C	XP_006717587.1:n.*2055G>C
XM_006717525.1:c.*2055G>C	XP_006717588.1:n.*2055G>C
NM_001330068.1:c.*2055G>C	NP_001316997.1:n.*2055G>C
XM_006717521.2:c.*2055G>C	XP_006717584.1:n.*2055G>C
XM_006717522.2:c.*2055G>C	XP_006717585.1:n.*2055G>C
XM_006717524.2:c.*2055G>C	XP_006717587.1:n.*2055G>C
XM_006717525.2:c.*2055G>C	XP_006717588.1:n.*2055G>C
XM_017016865.2:c.*2055G>C	XP_016872354.1:n.*2055G>C
XM_017016866.2:c.*2055G>C	XP_016872355.1:n.*2055G>C
NM_003873.6:c.*2055G>C	NP_003864.4:n.*2055G>C
NM_001244972.2:c.*2055G>C	NP_001231901.2:n.*2055G>C
NM_001244973.2:c.*2055G>C	NP_001231902.2:n.*2055G>C
NM_001330068.2:c.*2055G>C	NP_001316997.2:n.*2055G>C
NM_003873.7:c.*2055G>C MANE Select	NP_003864.5:n.*2055G>C
NR_045259.2:n.4909G>C