Canonical Allele Identifier: CA484986353
Gene: RPGRIP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.21793039C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21324880C>T , CM000676.2:g.21324880C>T GRCh38
NC_000014.8:g.21793039C>T , CM000676.1:g.21793039C>T GRCh37
NC_000014.7:g.20862879C>T NCBI36
NG_008933.1:g.41904C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400017.7:c.2025C>T MANE Select ENSP00000382895.2:p.Leu675=
ENST00000382933.8:c.689-2743C>T ENSP00000372391.4:n.689-2743C>T
ENST00000400017.6:c.2025C>T ENSP00000382895.2:p.Leu675=
ENST00000553500.5:n.328+155C>T
ENST00000553927.1:n.957C>T
ENST00000554303.1:c.411C>T ENSP00000450426.1:p.Leu137=
ENST00000555322.5:c.452C>T
ENST00000555489.5:c.218C>T ENSP00000451044.1:n.218C>T
ENST00000555587.5:c.450C>T ENSP00000451262.1:p.Leu150=
ENST00000556336.5:c.1682-2743C>T ENSP00000450445.1:n.1682-2743C>T
ENST00000557771.5:c.1911C>T ENSP00000451219.1:p.Leu637=
NM_020366.3:c.2025C>T NP_065099.3:p.Leu675=
XM_005267879.2:c.951C>T XP_005267936.1:p.Leu317=
XM_005267880.2:c.918C>T XP_005267937.1:p.Leu306=
XM_005267881.2:c.399C>T XP_005267938.1:p.Leu133=
XM_011536978.1:c.951C>T XP_011535280.1:p.Leu317=
XM_011536979.1:c.797-62C>T XP_011535281.1:n.797-62C>T
XM_011536980.1:c.796+155C>T XP_011535282.1:n.796+155C>T
XM_011536981.1:c.951C>T XP_011535283.1:p.Leu317=
XM_011536982.1:c.796+155C>T XP_011535284.1:n.796+155C>T
XM_011536983.1:c.1992C>T XP_011535285.1:p.Leu664=
XM_005267881.3:c.399C>T XP_005267938.1:p.Leu133=
XM_017021473.1:c.951C>T XP_016876962.1:p.Leu317=
XM_024449663.1:c.951C>T XP_024305431.1:p.Leu317=
XM_024449664.1:c.951C>T XP_024305432.1:p.Leu317=
XM_024449665.1:c.796+155C>T XP_024305433.1:n.796+155C>T
XM_024449666.1:c.796+155C>T XP_024305434.1:n.796+155C>T
NM_001377523.1:c.689-2743C>T NP_001364452.1:n.689-2743C>T
NM_001377948.1:c.951C>T NP_001364877.1:p.Leu317=
NM_001377949.1:c.796+155C>T NP_001364878.1:n.796+155C>T
NM_001377950.1:c.689-2743C>T NP_001364879.1:n.689-2743C>T
NM_001377951.1:c.191-2743C>T NP_001364880.1:n.191-2743C>T
NM_020366.4:c.2025C>T MANE Select NP_065099.3:p.Leu675=