Canonical Allele Identifier: CA99528441

Gene: NPFFR2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72137852A>G , CM000666.2:g.72137852A>G	GRCh38
NC_000004.11:g.73003569A>G , CM000666.1:g.73003569A>G	GRCh37
NC_000004.10:g.73222433A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308744.12:c.329-188A>G MANE Select	ENSP00000307822.7:n.329-188A>G
ENST00000308744.11:c.329-188A>G	ENSP00000307822.7:n.329-188A>G
ENST00000344413.6:c.-20-188A>G	ENSP00000340789.6:n.-20-188A>G
ENST00000308744.10:c.635-188A>G	ENSP00000307822.6:n.635-188A>G
ENST00000344413.5:c.300-188A>G	ENSP00000340789.5:n.300-188A>G
ENST00000358749.3:c.329-188A>G	ENSP00000351599.3:n.329-188A>G
ENST00000395999.5:c.338-188A>G	ENSP00000379321.1:n.338-188A>G
NM_001144756.1:c.338-188A>G	NP_001138228.1:n.338-188A>G
NM_004885.2:c.635-188A>G	NP_004876.2:n.635-188A>G
NM_053036.2:c.329-188A>G	NP_444264.1:n.329-188A>G
XM_011531554.1:c.-20-188A>G	XP_011529856.1:n.-20-188A>G
XM_011531554.2:c.-20-188A>G	XP_011529856.1:n.-20-188A>G
NM_001144756.2:c.338-188A>G	NP_001138228.1:n.338-188A>G
NM_004885.3:c.329-188A>G MANE Select	NP_004876.3:n.329-188A>G
NM_053036.3:c.329-188A>G	NP_444264.1:n.329-188A>G