Canonical Allele Identifier: CA2378115403

Gene: NRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14968231A= , CM000683.2:g.14968231A=	GRCh38
NC_000021.8:g.16340552A= , CM000683.1:g.16340552A=	GRCh37
NC_000021.7:g.15262423A=	NCBI36
NG_050643.1:g.102673T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318948.7:c.-39T= MANE Select	ENSP00000327213.4:n.-39T=
ENST00000638122.1:c.-39T=	ENSP00000490103.1:n.-39T=
ENST00000318948.6:c.-39T=	ENSP00000327213.4:n.-39T=
ENST00000400199.5:c.-39T=	ENSP00000383060.1:n.-39T=
ENST00000400202.5:c.-39T=	ENSP00000383063.1:n.-39T=
ENST00000411932.1:c.-39T=	ENSP00000412114.1:n.-39T=
NM_003489.3:c.-39T=	NP_003480.2:n.-39T=
XM_005261063.2:c.-39T=	XP_005261120.1:n.-39T=
XM_005261065.2:c.-39T=	XP_005261122.1:n.-39T=
XM_011529747.1:c.-39T=	XP_011528049.1:n.-39T=
XM_011529748.1:c.-39T=	XP_011528050.1:n.-39T=
XM_011529749.1:c.-39T=	XP_011528051.1:n.-39T=
XM_011529750.1:c.-39T=	XP_011528052.1:n.-39T=
XM_011529751.1:c.-39T=	XP_011528053.1:n.-39T=
XM_011529752.1:c.-39T=	XP_011528054.1:n.-39T=
XM_005261063.3:c.-39T=	XP_005261120.1:n.-39T=
XM_005261065.3:c.-39T=	XP_005261122.1:n.-39T=
XM_011529748.2:c.-39T=	XP_011528050.1:n.-39T=
XM_011529749.2:c.-39T=	XP_011528051.1:n.-39T=
XM_011529751.2:c.-39T=	XP_011528053.1:n.-39T=
XM_017028473.1:c.-39T=	XP_016883962.1:n.-39T=
XM_017028474.1:c.-39T=	XP_016883963.1:n.-39T=
XM_017028475.1:c.-39T=	XP_016883964.1:n.-39T=
XM_017028476.1:c.-39T=	XP_016883965.1:n.-39T=
NM_003489.4:c.-39T= MANE Select	NP_003480.2:n.-39T=