Canonical Allele Identifier: CA344043280

Gene: CRB1

Linked Data

• gnomAD v4: 1-197434754-G-C
• MyVariant Identifiers: chr1:g.197403884G>C (hg19) ; chr1:g.197434754G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434754G>C , CM000663.2:g.197434754G>C	GRCh38
NC_000001.10:g.197403884G>C , CM000663.1:g.197403884G>C	GRCh37
NC_000001.9:g.195670507G>C	NCBI36
NG_008483.1:g.171477G>C
NG_008483.2:g.238293G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2891G>C MANE Select	ENSP00000356370.3:p.Arg964Thr
ENST00000638467.1:c.2891G>C	ENSP00000491102.1:p.Arg964Thr
ENST00000681519.1:c.1772G>C	ENSP00000505267.1:p.Arg591Thr
ENST00000367397.1:c.1034G>C	ENSP00000356367.1:p.Arg345Thr
ENST00000367399.6:c.2555G>C	ENSP00000356369.2:p.Arg852Thr
ENST00000367400.7:c.2891G>C	ENSP00000356370.3:p.Arg964Thr
ENST00000484075.5:c.2891G>C	ENSP00000433932.1:p.Arg964Thr
ENST00000535699.5:c.2819G>C	ENSP00000438786.1:p.Arg940Thr
ENST00000538660.5:c.2129-846G>C	ENSP00000438091.1:n.2129-846G>C
NM_001193640.1:c.2555G>C	NP_001180569.1:p.Arg852Thr
NM_001257965.1:c.2819G>C	NP_001244894.1:p.Arg940Thr
NM_001257966.1:c.2129-846G>C	NP_001244895.1:n.2129-846G>C
NM_201253.2:c.2891G>C	NP_957705.1:p.Arg964Thr
NR_047563.1:n.2892G>C
NR_047564.1:n.3100G>C
XM_011509365.1:c.2891G>C	XP_011507667.1:p.Arg964Thr
XM_011509366.1:c.2891G>C	XP_011507668.1:p.Arg964Thr
XM_011509367.1:c.2891G>C	XP_011507669.1:p.Arg964Thr
XM_011509368.1:c.2309G>C	XP_011507670.1:p.Arg770Thr
XM_011509369.1:c.1334G>C	XP_011507671.1:p.Arg445Thr
XM_011509365.2:c.2891G>C	XP_011507667.1:p.Arg964Thr
XM_011509369.2:c.1334G>C	XP_011507671.1:p.Arg445Thr
XM_017000851.1:c.2048G>C	XP_016856340.1:p.Arg683Thr
XM_017000852.1:c.3026G>C	XP_016856341.1:p.Arg1009Thr
NM_201253.3:c.2891G>C MANE Select	NP_957705.1:p.Arg964Thr
NM_001193640.2:c.2555G>C	NP_001180569.1:p.Arg852Thr
NM_001257965.2:c.2819G>C	NP_001244894.1:p.Arg940Thr
NR_047563.2:n.2844G>C
NR_047564.2:n.3052G>C
NM_001257966.2:c.2129-846G>C	NP_001244895.1:n.2129-846G>C