Canonical Allele Identifier: CA344047030

Gene: CRB1

Linked Data

• gnomAD v4: 1-197435166-A-T
• MyVariant Identifiers: chr1:g.197404296A>T (hg19) ; chr1:g.197435166A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435166A>T , CM000663.2:g.197435166A>T	GRCh38
NC_000001.10:g.197404296A>T , CM000663.1:g.197404296A>T	GRCh37
NC_000001.9:g.195670919A>T	NCBI36
NG_008483.1:g.171889A>T
NG_008483.2:g.238705A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.3303A>T MANE Select	ENSP00000356370.3:p.Glu1101Asp
ENST00000638467.1:c.3303A>T	ENSP00000491102.1:p.Glu1101Asp
ENST00000681519.1:c.2184A>T	ENSP00000505267.1:p.Glu728Asp
ENST00000367397.1:c.1446A>T	ENSP00000356367.1:p.Glu482Asp
ENST00000367399.6:c.2967A>T	ENSP00000356369.2:p.Glu989Asp
ENST00000367400.7:c.3303A>T	ENSP00000356370.3:p.Glu1101Asp
ENST00000484075.5:c.3303A>T	ENSP00000433932.1:p.Glu1101Asp
ENST00000535699.5:c.3231A>T	ENSP00000438786.1:p.Glu1077Asp
ENST00000538660.5:c.2129-434A>T	ENSP00000438091.1:n.2129-434A>T
NM_001193640.1:c.2967A>T	NP_001180569.1:p.Glu989Asp
NM_001257965.1:c.3231A>T	NP_001244894.1:p.Glu1077Asp
NM_001257966.1:c.2129-434A>T	NP_001244895.1:n.2129-434A>T
NM_201253.2:c.3303A>T	NP_957705.1:p.Glu1101Asp
NR_047563.1:n.3304A>T
NR_047564.1:n.3512A>T
XM_011509365.1:c.3303A>T	XP_011507667.1:p.Glu1101Asp
XM_011509366.1:c.3303A>T	XP_011507668.1:p.Glu1101Asp
XM_011509367.1:c.3303A>T	XP_011507669.1:p.Glu1101Asp
XM_011509368.1:c.2721A>T	XP_011507670.1:p.Glu907Asp
XM_011509369.1:c.1746A>T	XP_011507671.1:p.Glu582Asp
XM_011509365.2:c.3303A>T	XP_011507667.1:p.Glu1101Asp
XM_011509369.2:c.1746A>T	XP_011507671.1:p.Glu582Asp
XM_017000851.1:c.2460A>T	XP_016856340.1:p.Glu820Asp
XM_017000852.1:c.3438A>T	XP_016856341.1:p.Glu1146Asp
NM_201253.3:c.3303A>T MANE Select	NP_957705.1:p.Glu1101Asp
NM_001193640.2:c.2967A>T	NP_001180569.1:p.Glu989Asp
NM_001257965.2:c.3231A>T	NP_001244894.1:p.Glu1077Asp
NR_047563.2:n.3256A>T
NR_047564.2:n.3464A>T
NM_001257966.2:c.2129-434A>T	NP_001244895.1:n.2129-434A>T