Canonical Allele Identifier: CA344031371

Gene: CRB1

Linked Data

• gnomAD v4: 1-197421366-G-C
• MyVariant Identifiers: chr1:g.197390496G>C (hg19) ; chr1:g.197421366G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421366G>C , CM000663.2:g.197421366G>C	GRCh38
NC_000001.10:g.197390496G>C , CM000663.1:g.197390496G>C	GRCh37
NC_000001.9:g.195657119G>C	NCBI36
NG_008483.1:g.158089G>C
NG_008483.2:g.224905G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.1538G>C MANE Select	ENSP00000356370.3:p.Arg513Thr
ENST00000638467.1:c.1538G>C	ENSP00000491102.1:p.Arg513Thr
ENST00000681519.1:c.419G>C	ENSP00000505267.1:p.Arg140Thr
ENST00000367397.1:c.-320G>C	ENSP00000356367.1:n.-320G>C
ENST00000367399.6:c.1202G>C	ENSP00000356369.2:p.Arg401Thr
ENST00000367400.7:c.1538G>C	ENSP00000356370.3:p.Arg513Thr
ENST00000476483.1:n.498G>C
ENST00000484075.5:c.1538G>C	ENSP00000433932.1:p.Arg513Thr
ENST00000535699.5:c.1331G>C	ENSP00000438786.1:p.Arg444Thr
ENST00000538660.5:c.1538G>C	ENSP00000438091.1:p.Arg513Thr
NM_001193640.1:c.1202G>C	NP_001180569.1:p.Arg401Thr
NM_001257965.1:c.1331G>C	NP_001244894.1:p.Arg444Thr
NM_001257966.1:c.1538G>C	NP_001244895.1:p.Arg513Thr
NM_201253.2:c.1538G>C	NP_957705.1:p.Arg513Thr
NR_047563.1:n.1747G>C
NR_047564.1:n.1747G>C
XM_011509365.1:c.1538G>C	XP_011507667.1:p.Arg513Thr
XM_011509366.1:c.1538G>C	XP_011507668.1:p.Arg513Thr
XM_011509367.1:c.1538G>C	XP_011507669.1:p.Arg513Thr
XM_011509368.1:c.956G>C	XP_011507670.1:p.Arg319Thr
XM_011509369.1:c.-20G>C	XP_011507671.1:n.-20G>C
XM_011509365.2:c.1538G>C	XP_011507667.1:p.Arg513Thr
XM_011509369.2:c.-20G>C	XP_011507671.1:n.-20G>C
XM_017000851.1:c.695G>C	XP_016856340.1:p.Arg232Thr
XM_017000852.1:c.1538G>C	XP_016856341.1:p.Arg513Thr
NM_201253.3:c.1538G>C MANE Select	NP_957705.1:p.Arg513Thr
NM_001193640.2:c.1202G>C	NP_001180569.1:p.Arg401Thr
NM_001257965.2:c.1331G>C	NP_001244894.1:p.Arg444Thr
NR_047563.2:n.1699G>C
NR_047564.2:n.1699G>C
NM_001257966.2:c.1538G>C	NP_001244895.1:p.Arg513Thr