Canonical Allele Identifier: CA9515949

Gene: RTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45488492G>C , CM000681.2:g.45488492G>C	GRCh38
NC_000019.9:g.45991750G>C , CM000681.1:g.45991750G>C	GRCh37
NC_000019.8:g.50683590G>C	NCBI36
NG_032157.1:g.13562C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005619.5:c.1476C>G MANE Select	NP_005610.1:p.Pro492=
ENST00000245923.9:c.1476C>G MANE Select	ENSP00000245923.3:p.Pro492=
NM_005619.4:c.1476C>G	NP_005610.1:p.Pro492=
NM_206900.2:c.1257C>G	NP_996783.1:p.Pro419=
NM_206900.3:c.1257C>G	NP_996783.1:p.Pro419=
NM_206901.2:c.456C>G	NP_996784.1:p.Pro152=
NM_206901.3:c.456C>G	NP_996784.1:p.Pro152=
ENST00000245923.8:c.1476C>G	ENSP00000245923.3:p.Pro492=
ENST00000344680.8:c.1257C>G	ENSP00000345127.3:p.Pro419=
ENST00000430715.6:c.456C>G	ENSP00000398178.1:p.Pro152=
ENST00000587597.5:c.*20C>G	ENSP00000468144.1:n.*20C>G
ENST00000588036.5:n.314C>G
ENST00000590526.5:c.654C>G	ENSP00000466619.1:p.Pro218=
ENST00000590746.5:n.62-2379C>G
ENST00000591286.5:c.*474C>G	ENSP00000467863.1:n.*474C>G
ENST00000591789.1:n.482C>G
ENST00000593129.1:n.352C>G
ENST00000593187.5:n.78C>G