Canonical Allele Identifier: CA388862927
Gene: RPGRIP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.21780658T>G (hg19) chr14:g.21312499T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21312499T>G , CM000676.2:g.21312499T>G GRCh38
NC_000014.8:g.21780658T>G , CM000676.1:g.21780658T>G GRCh37
NC_000014.7:g.20850498T>G NCBI36
NG_008933.1:g.29523T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1144T>G MANE Select ENSP00000382895.2:p.Leu382Val
ENST00000400017.6:c.1144T>G ENSP00000382895.2:p.Leu382Val
ENST00000556336.5:c.1063T>G ENSP00000450445.1:p.Leu355Val
ENST00000557771.5:c.1063T>G ENSP00000451219.1:p.Leu355Val
NM_020366.3:c.1144T>G NP_065099.3:p.Leu382Val
XM_011536983.1:c.1111T>G XP_011535285.1:p.Leu371Val
NM_020366.4:c.1144T>G MANE Select NP_065099.3:p.Leu382Val
Search 100 bp 5'
Search 100 bp 3'