Canonical Allele Identifier: CA422808477
Gene: CRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.197390401A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421271A>G , CM000663.2:g.197421271A>G GRCh38
NC_000001.10:g.197390401A>G , CM000663.1:g.197390401A>G GRCh37
NC_000001.9:g.195657024A>G NCBI36
NG_008483.1:g.157994A>G
NG_008483.2:g.224810A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367400.8:c.1443A>G MANE Select ENSP00000356370.3:p.Glu481=
ENST00000638467.1:c.1443A>G ENSP00000491102.1:p.Glu481=
ENST00000681519.1:c.324A>G ENSP00000505267.1:p.Glu108=
ENST00000367397.1:c.-415A>G ENSP00000356367.1:n.-415A>G
ENST00000367399.6:c.1107A>G ENSP00000356369.2:p.Glu369=
ENST00000367400.7:c.1443A>G ENSP00000356370.3:p.Glu481=
ENST00000476483.1:n.403A>G
ENST00000484075.5:c.1443A>G ENSP00000433932.1:p.Glu481=
ENST00000535699.5:c.1236A>G ENSP00000438786.1:p.Glu412=
ENST00000538660.5:c.1443A>G ENSP00000438091.1:p.Glu481=
NM_001193640.1:c.1107A>G NP_001180569.1:p.Glu369=
NM_001257965.1:c.1236A>G NP_001244894.1:p.Glu412=
NM_001257966.1:c.1443A>G NP_001244895.1:p.Glu481=
NM_201253.2:c.1443A>G NP_957705.1:p.Glu481=
NR_047563.1:n.1652A>G
NR_047564.1:n.1652A>G
XM_011509365.1:c.1443A>G XP_011507667.1:p.Glu481=
XM_011509366.1:c.1443A>G XP_011507668.1:p.Glu481=
XM_011509367.1:c.1443A>G XP_011507669.1:p.Glu481=
XM_011509368.1:c.861A>G XP_011507670.1:p.Glu287=
XM_011509369.1:c.-115A>G XP_011507671.1:n.-115A>G
XM_011509365.2:c.1443A>G XP_011507667.1:p.Glu481=
XM_011509369.2:c.-115A>G XP_011507671.1:n.-115A>G
XM_017000851.1:c.600A>G XP_016856340.1:p.Glu200=
XM_017000852.1:c.1443A>G XP_016856341.1:p.Glu481=
NM_201253.3:c.1443A>G MANE Select NP_957705.1:p.Glu481=
NM_001193640.2:c.1107A>G NP_001180569.1:p.Glu369=
NM_001257965.2:c.1236A>G NP_001244894.1:p.Glu412=
NR_047563.2:n.1604A>G
NR_047564.2:n.1604A>G
NM_001257966.2:c.1443A>G NP_001244895.1:p.Glu481=