Canonical Allele Identifier: CA11781659

Gene: NPFFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72097303T>G , CM000666.2:g.72097303T>G	GRCh38
NC_000004.11:g.72963020T>G , CM000666.1:g.72963020T>G	GRCh37
NC_000004.10:g.73181884T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004885.3:c.-7-31282T>G MANE Select	NP_004876.3:n.-7-31282T>G
ENST00000308744.12:c.-7-31282T>G MANE Select	ENSP00000307822.7:n.-7-31282T>G
NM_001144756.1:c.2+28280T>G	NP_001138228.1:n.2+28280T>G
NM_001144756.2:c.2+28280T>G	NP_001138228.1:n.2+28280T>G
NM_004885.2:c.300-31282T>G	NP_004876.2:n.300-31282T>G
NM_053036.2:c.-7-31282T>G	NP_444264.1:n.-7-31282T>G
NM_053036.3:c.-7-31282T>G	NP_444264.1:n.-7-31282T>G
ENST00000308744.10:c.300-31282T>G	ENSP00000307822.6:n.300-31282T>G
ENST00000308744.11:c.-7-31282T>G	ENSP00000307822.7:n.-7-31282T>G
ENST00000344413.5:c.300-40737T>G	ENSP00000340789.5:n.300-40737T>G
ENST00000344413.6:c.-20-40737T>G	ENSP00000340789.6:n.-20-40737T>G
ENST00000358749.3:c.-7-31282T>G	ENSP00000351599.3:n.-7-31282T>G
ENST00000395999.5:c.2+28280T>G	ENSP00000379321.1:n.2+28280T>G
XM_011531554.1:c.-20-40737T>G	XP_011529856.1:n.-20-40737T>G
XM_011531554.2:c.-20-40737T>G	XP_011529856.1:n.-20-40737T>G