Canonical Allele Identifier: CA7088875
Gene: RPGRIP1 HGNC NCBI

Linked Data

dbSNP Id: rs756520616
ExAC: 14:21780627 A / G
gnomAD v2: 14-21780627-A-G
gnomAD v4: 14-21312468-A-G
MyVariant Identifiers: chr14:g.21780627A>G (hg19) chr14:g.21312468A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21312468A>G , CM000676.2:g.21312468A>G GRCh38
NC_000014.8:g.21780627A>G , CM000676.1:g.21780627A>G GRCh37
NC_000014.7:g.20850467A>G NCBI36
NG_008933.1:g.29492A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.1113A>G MANE Select ENSP00000382895.2:p.Arg371=
ENST00000400017.6:c.1113A>G ENSP00000382895.2:p.Arg371=
ENST00000556336.5:c.1032A>G ENSP00000450445.1:p.Arg344=
ENST00000557771.5:c.1032A>G ENSP00000451219.1:p.Arg344=
NM_020366.3:c.1113A>G NP_065099.3:p.Arg371=
XM_011536983.1:c.1080A>G XP_011535285.1:p.Arg360=
NM_020366.4:c.1113A>G MANE Select NP_065099.3:p.Arg371=
Search 100 bp 5'
Search 100 bp 3'