Canonical Allele Identifier: CA2563579147

Gene: NRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14968252_14968253insTTTG , CM000683.2:g.14968252_14968253insTTTG	GRCh38
NC_000021.8:g.16340573_16340574insTTTG , CM000683.1:g.16340573_16340574insTTTG	GRCh37
NC_000021.7:g.15262444_15262445insTTTG	NCBI36
NG_050643.1:g.102651_102652insCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318948.7:c.-61_-60insCAAA MANE Select	ENSP00000327213.4:n.-61_-60insCAAA
ENST00000638122.1:c.-61_-60insCAAA	ENSP00000490103.1:n.-61_-60insCAAA
ENST00000318948.6:c.-61_-60insCAAA	ENSP00000327213.4:n.-61_-60insCAAA
ENST00000400199.5:c.-61_-60insCAAA	ENSP00000383060.1:n.-61_-60insCAAA
ENST00000400202.5:c.-61_-60insCAAA	ENSP00000383063.1:n.-61_-60insCAAA
ENST00000411932.1:c.-61_-60insCAAA	ENSP00000412114.1:n.-61_-60insCAAA
NM_003489.3:c.-61_-60insCAAA	NP_003480.2:n.-61_-60insCAAA
XM_005261063.2:c.-61_-60insCAAA	XP_005261120.1:n.-61_-60insCAAA
XM_005261065.2:c.-61_-60insCAAA	XP_005261122.1:n.-61_-60insCAAA
XM_011529747.1:c.-61_-60insCAAA	XP_011528049.1:n.-61_-60insCAAA
XM_011529748.1:c.-61_-60insCAAA	XP_011528050.1:n.-61_-60insCAAA
XM_011529749.1:c.-61_-60insCAAA	XP_011528051.1:n.-61_-60insCAAA
XM_011529750.1:c.-61_-60insCAAA	XP_011528052.1:n.-61_-60insCAAA
XM_011529751.1:c.-61_-60insCAAA	XP_011528053.1:n.-61_-60insCAAA
XM_011529752.1:c.-61_-60insCAAA	XP_011528054.1:n.-61_-60insCAAA
XM_005261063.3:c.-61_-60insCAAA	XP_005261120.1:n.-61_-60insCAAA
XM_005261065.3:c.-61_-60insCAAA	XP_005261122.1:n.-61_-60insCAAA
XM_011529748.2:c.-61_-60insCAAA	XP_011528050.1:n.-61_-60insCAAA
XM_011529749.2:c.-61_-60insCAAA	XP_011528051.1:n.-61_-60insCAAA
XM_011529751.2:c.-61_-60insCAAA	XP_011528053.1:n.-61_-60insCAAA
XM_017028473.1:c.-61_-60insCAAA	XP_016883962.1:n.-61_-60insCAAA
XM_017028474.1:c.-61_-60insCAAA	XP_016883963.1:n.-61_-60insCAAA
XM_017028475.1:c.-61_-60insCAAA	XP_016883964.1:n.-61_-60insCAAA
XM_017028476.1:c.-61_-60insCAAA	XP_016883965.1:n.-61_-60insCAAA
NM_003489.4:c.-61_-60insCAAA MANE Select	NP_003480.2:n.-61_-60insCAAA