Canonical Allele Identifier: CA344047025

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404294G>C (hg19) ; chr1:g.197435164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435164G>C , CM000663.2:g.197435164G>C	GRCh38
NC_000001.10:g.197404294G>C , CM000663.1:g.197404294G>C	GRCh37
NC_000001.9:g.195670917G>C	NCBI36
NG_008483.1:g.171887G>C
NG_008483.2:g.238703G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.3301G>C MANE Select	ENSP00000356370.3:p.Glu1101Gln
ENST00000638467.1:c.3301G>C	ENSP00000491102.1:p.Glu1101Gln
ENST00000681519.1:c.2182G>C	ENSP00000505267.1:p.Glu728Gln
ENST00000367397.1:c.1444G>C	ENSP00000356367.1:p.Glu482Gln
ENST00000367399.6:c.2965G>C	ENSP00000356369.2:p.Glu989Gln
ENST00000367400.7:c.3301G>C	ENSP00000356370.3:p.Glu1101Gln
ENST00000484075.5:c.3301G>C	ENSP00000433932.1:p.Glu1101Gln
ENST00000535699.5:c.3229G>C	ENSP00000438786.1:p.Glu1077Gln
ENST00000538660.5:c.2129-436G>C	ENSP00000438091.1:n.2129-436G>C
NM_001193640.1:c.2965G>C	NP_001180569.1:p.Glu989Gln
NM_001257965.1:c.3229G>C	NP_001244894.1:p.Glu1077Gln
NM_001257966.1:c.2129-436G>C	NP_001244895.1:n.2129-436G>C
NM_201253.2:c.3301G>C	NP_957705.1:p.Glu1101Gln
NR_047563.1:n.3302G>C
NR_047564.1:n.3510G>C
XM_011509365.1:c.3301G>C	XP_011507667.1:p.Glu1101Gln
XM_011509366.1:c.3301G>C	XP_011507668.1:p.Glu1101Gln
XM_011509367.1:c.3301G>C	XP_011507669.1:p.Glu1101Gln
XM_011509368.1:c.2719G>C	XP_011507670.1:p.Glu907Gln
XM_011509369.1:c.1744G>C	XP_011507671.1:p.Glu582Gln
XM_011509365.2:c.3301G>C	XP_011507667.1:p.Glu1101Gln
XM_011509369.2:c.1744G>C	XP_011507671.1:p.Glu582Gln
XM_017000851.1:c.2458G>C	XP_016856340.1:p.Glu820Gln
XM_017000852.1:c.3436G>C	XP_016856341.1:p.Glu1146Gln
NM_201253.3:c.3301G>C MANE Select	NP_957705.1:p.Glu1101Gln
NM_001193640.2:c.2965G>C	NP_001180569.1:p.Glu989Gln
NM_001257965.2:c.3229G>C	NP_001244894.1:p.Glu1077Gln
NR_047563.2:n.3254G>C
NR_047564.2:n.3462G>C
NM_001257966.2:c.2129-436G>C	NP_001244895.1:n.2129-436G>C