Canonical Allele Identifier: CA1323032199

Gene: NRP2

Genomic Alleles

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

Transcript Alleles

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