Canonical Allele Identifier: CA2649673034

Gene: CRB1

Linked Data

• gnomAD v4: 1-197478018-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197478020del , CM000663.2:g.197478020del	GRCh38
NC_000001.10:g.197447150del , CM000663.1:g.197447150del	GRCh37
NC_000001.9:g.195713773del	NCBI36
NG_008483.1:g.214743del
NG_008483.2:g.281559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.*141del MANE Select	ENSP00000356370.3:n.*141del
ENST00000367400.7:c.*141del	ENSP00000356370.3:n.*141del
ENST00000448952.1:c.596del	ENSP00000395407.1:n.596del
ENST00000484075.5:c.*473del	ENSP00000433932.1:n.*473del
ENST00000535699.5:c.*141del	ENSP00000438786.1:n.*141del
ENST00000538660.5:c.*141del	ENSP00000438091.1:n.*141del
NM_001193640.1:c.*141del	NP_001180569.1:n.*141del
NM_001257965.1:c.*141del	NP_001244894.1:n.*141del
NM_001257966.1:c.*141del	NP_001244895.1:n.*141del
NM_201253.2:c.*141del	NP_957705.1:n.*141del
NR_047563.1:n.4363del
NR_047564.1:n.4813del
XM_011509366.1:c.*467del	XP_011507668.1:n.*467del
XM_011509367.1:c.*341del	XP_011507669.1:n.*341del
XM_011509368.1:c.*141del	XP_011507670.1:n.*141del
XM_011509369.1:c.*141del	XP_011507671.1:n.*141del
XM_011509369.2:c.*141del	XP_011507671.1:n.*141del
XM_017000851.1:c.*141del	XP_016856340.1:n.*141del
XM_017000852.1:c.*141del	XP_016856341.1:n.*141del
NM_201253.3:c.*141del MANE Select	NP_957705.1:n.*141del
NM_001193640.2:c.*141del	NP_001180569.1:n.*141del
NM_001257965.2:c.*141del	NP_001244894.1:n.*141del
NR_047563.2:n.4315del
NR_047564.2:n.4765del
NM_001257966.2:c.*141del	NP_001244895.1:n.*141del