Canonical Allele Identifier: CA410712168

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20229913G>A (hg19) ; chr22:g.20242390G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242390G>A , CM000684.2:g.20242390G>A	GRCh38
NC_000022.10:g.20229913G>A , CM000684.1:g.20229913G>A	GRCh37
NC_000022.9:g.18609913G>A	NCBI36
NG_012176.1:g.30904C>T
NG_012176.2:g.30904C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.743C>T MANE Select	ENSP00000043402.7:p.Pro248Leu
ENST00000043402.7:c.743C>T	ENSP00000043402.7:p.Pro248Leu
ENST00000416372.5:c.802C>T
ENST00000425986.1:c.1000C>T
NM_023004.5:c.743C>T	NP_075380.1:p.Pro248Leu
NM_023004.6:c.743C>T MANE Select	NP_075380.1:p.Pro248Leu