Canonical Allele Identifier: CA344043729

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403928G>C (hg19) ; chr1:g.197434798G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434798G>C , CM000663.2:g.197434798G>C	GRCh38
NC_000001.10:g.197403928G>C , CM000663.1:g.197403928G>C	GRCh37
NC_000001.9:g.195670551G>C	NCBI36
NG_008483.1:g.171521G>C
NG_008483.2:g.238337G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2935G>C MANE Select	ENSP00000356370.3:p.Gly979Arg
ENST00000638467.1:c.2935G>C	ENSP00000491102.1:p.Gly979Arg
ENST00000681519.1:c.1816G>C	ENSP00000505267.1:p.Gly606Arg
ENST00000367397.1:c.1078G>C	ENSP00000356367.1:p.Gly360Arg
ENST00000367399.6:c.2599G>C	ENSP00000356369.2:p.Gly867Arg
ENST00000367400.7:c.2935G>C	ENSP00000356370.3:p.Gly979Arg
ENST00000484075.5:c.2935G>C	ENSP00000433932.1:p.Gly979Arg
ENST00000535699.5:c.2863G>C	ENSP00000438786.1:p.Gly955Arg
ENST00000538660.5:c.2129-802G>C	ENSP00000438091.1:n.2129-802G>C
NM_001193640.1:c.2599G>C	NP_001180569.1:p.Gly867Arg
NM_001257965.1:c.2863G>C	NP_001244894.1:p.Gly955Arg
NM_001257966.1:c.2129-802G>C	NP_001244895.1:n.2129-802G>C
NM_201253.2:c.2935G>C	NP_957705.1:p.Gly979Arg
NR_047563.1:n.2936G>C
NR_047564.1:n.3144G>C
XM_011509365.1:c.2935G>C	XP_011507667.1:p.Gly979Arg
XM_011509366.1:c.2935G>C	XP_011507668.1:p.Gly979Arg
XM_011509367.1:c.2935G>C	XP_011507669.1:p.Gly979Arg
XM_011509368.1:c.2353G>C	XP_011507670.1:p.Gly785Arg
XM_011509369.1:c.1378G>C	XP_011507671.1:p.Gly460Arg
XM_011509365.2:c.2935G>C	XP_011507667.1:p.Gly979Arg
XM_011509369.2:c.1378G>C	XP_011507671.1:p.Gly460Arg
XM_017000851.1:c.2092G>C	XP_016856340.1:p.Gly698Arg
XM_017000852.1:c.3070G>C	XP_016856341.1:p.Gly1024Arg
NM_201253.3:c.2935G>C MANE Select	NP_957705.1:p.Gly979Arg
NM_001193640.2:c.2599G>C	NP_001180569.1:p.Gly867Arg
NM_001257965.2:c.2863G>C	NP_001244894.1:p.Gly955Arg
NR_047563.2:n.2888G>C
NR_047564.2:n.3096G>C
NM_001257966.2:c.2129-802G>C	NP_001244895.1:n.2129-802G>C