Canonical Allele Identifier: CA344084316

Gene: CRB1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197356840G>C , CM000663.2:g.197356840G>C	GRCh38
NC_000001.10:g.197325970G>C , CM000663.1:g.197325970G>C	GRCh37
NC_000001.9:g.195592593G>C	NCBI36
NG_008483.1:g.93563G>C
NG_008483.2:g.160379G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.998G>C MANE Select	ENSP00000356370.3:p.Gly333Ala
ENST00000638467.1:c.998G>C	ENSP00000491102.1:p.Gly333Ala
ENST00000367399.6:c.662G>C	ENSP00000356369.2:p.Gly221Ala
ENST00000367400.7:c.998G>C	ENSP00000356370.3:p.Gly333Ala
ENST00000475659.1:n.1135G>C
ENST00000484075.5:c.998G>C	ENSP00000433932.1:p.Gly333Ala
ENST00000535699.5:c.791G>C	ENSP00000438786.1:p.Gly264Ala
ENST00000538660.5:c.998G>C	ENSP00000438091.1:p.Gly333Ala
NM_001193640.1:c.662G>C	NP_001180569.1:p.Gly221Ala
NM_001257965.1:c.791G>C	NP_001244894.1:p.Gly264Ala
NM_001257966.1:c.998G>C	NP_001244895.1:p.Gly333Ala
NM_201253.2:c.998G>C	NP_957705.1:p.Gly333Ala
NR_047563.1:n.1207G>C
NR_047564.1:n.1207G>C
XM_011509365.1:c.998G>C	XP_011507667.1:p.Gly333Ala
XM_011509366.1:c.998G>C	XP_011507668.1:p.Gly333Ala
XM_011509367.1:c.998G>C	XP_011507669.1:p.Gly333Ala
XM_011509368.1:c.416G>C	XP_011507670.1:p.Gly139Ala
XM_011509365.2:c.998G>C	XP_011507667.1:p.Gly333Ala
XM_017000851.1:c.155G>C	XP_016856340.1:p.Gly52Ala
XM_017000852.1:c.998G>C	XP_016856341.1:p.Gly333Ala
NM_201253.3:c.998G>C MANE Select	NP_957705.1:p.Gly333Ala
NM_001193640.2:c.662G>C	NP_001180569.1:p.Gly221Ala
NM_001257965.2:c.791G>C	NP_001244894.1:p.Gly264Ala
NR_047563.2:n.1159G>C
NR_047564.2:n.1159G>C
NM_001257966.2:c.998G>C	NP_001244895.1:p.Gly333Ala