Canonical Allele Identifier: CA763780038

Gene: NRP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.205797619A>T , CM000664.2:g.205797619A>T	GRCh38
NC_000002.11:g.206662343A>T , CM000664.1:g.206662343A>T	GRCh37
NC_000002.10:g.206370588A>T	NCBI36
NG_029567.1:g.120120A>T
NG_029567.2:g.120120A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357785.10:c.*2561A>T MANE Select	ENSP00000350432.5:n.*2561A>T
ENST00000360409.7:c.*2561A>T	ENSP00000353582.3:n.*2561A>T
NM_003872.2:c.*2561A>T	NP_003863.2:n.*2561A>T
NM_201266.1:c.*2561A>T	NP_957718.1:n.*2561A>T
NM_201279.1:c.*2561A>T	NP_958436.1:n.*2561A>T
XM_005246933.2:c.*2561A>T	XP_005246990.2:n.*2561A>T
XM_005246934.2:c.*2561A>T	XP_005246991.2:n.*2561A>T
XR_923055.1:n.5921A>T
XR_923055.3:n.5127A>T
NM_003872.3:c.*2561A>T MANE Select	NP_003863.2:n.*2561A>T
NM_201266.2:c.*2561A>T	NP_957718.1:n.*2561A>T
NM_201279.2:c.*2561A>T	NP_958436.1:n.*2561A>T