Canonical Allele Identifier: CA1323032201

Gene: NRP2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.205787576C>A , CM000664.2:g.205787576C>A	GRCh38
NC_000002.11:g.206652300C>A , CM000664.1:g.206652300C>A	GRCh37
NC_000002.10:g.206360545C>A	NCBI36
NG_029567.1:g.110077C>A
NG_029567.2:g.110077C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357785.10:c.2426-4659C>A MANE Select	ENSP00000350432.5:n.2426-4659C>A
ENST00000357785.9:c.2426-4659C>A	ENSP00000350432.5:n.2426-4659C>A
ENST00000360409.7:c.2441-4659C>A	ENSP00000353582.3:n.2441-4659C>A
ENST00000412873.2:c.2426-7178C>A	ENSP00000407626.2:n.2426-7178C>A
ENST00000467850.1:n.276-4659C>A
NM_003872.2:c.2426-4659C>A	NP_003863.2:n.2426-4659C>A
NM_201266.1:c.2441-4659C>A	NP_957718.1:n.2441-4659C>A
NM_201279.1:c.2426-7178C>A	NP_958436.1:n.2426-7178C>A
XM_005246933.2:c.2441-4659C>A	XP_005246990.2:n.2441-4659C>A
XM_005246934.2:c.2441-4659C>A	XP_005246991.2:n.2441-4659C>A
XR_923055.1:n.3005-4659C>A
XM_017005187.2:c.*2079C>A	XP_016860676.1:n.*2079C>A
XM_017005188.2:c.*2079C>A	XP_016860677.1:n.*2079C>A
XR_923055.3:n.2211-4659C>A
NM_003872.3:c.2426-4659C>A MANE Select	NP_003863.2:n.2426-4659C>A
NM_201266.2:c.2441-4659C>A	NP_957718.1:n.2441-4659C>A
NM_201279.2:c.2426-7178C>A	NP_958436.1:n.2426-7178C>A