Canonical Allele Identifier: CA2573974804

Gene: CRB1

Linked Data

• gnomAD v4: 1-197477955-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477955C>A , CM000663.2:g.197477955C>A	GRCh38
NC_000001.10:g.197447085C>A , CM000663.1:g.197447085C>A	GRCh37
NC_000001.9:g.195713708C>A	NCBI36
NG_008483.1:g.214678C>A
NG_008483.2:g.281494C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.*76C>A MANE Select	ENSP00000356370.3:n.*76C>A
ENST00000367400.7:c.*76C>A	ENSP00000356370.3:n.*76C>A
ENST00000448952.1:c.531C>A	ENSP00000395407.1:n.531C>A
ENST00000484075.5:c.*408C>A	ENSP00000433932.1:n.*408C>A
ENST00000535699.5:c.*76C>A	ENSP00000438786.1:n.*76C>A
ENST00000538660.5:c.*76C>A	ENSP00000438091.1:n.*76C>A
NM_001193640.1:c.*76C>A	NP_001180569.1:n.*76C>A
NM_001257965.1:c.*76C>A	NP_001244894.1:n.*76C>A
NM_001257966.1:c.*76C>A	NP_001244895.1:n.*76C>A
NM_201253.2:c.*76C>A	NP_957705.1:n.*76C>A
NR_047563.1:n.4298C>A
NR_047564.1:n.4748C>A
XM_011509366.1:c.*402C>A	XP_011507668.1:n.*402C>A
XM_011509367.1:c.*276C>A	XP_011507669.1:n.*276C>A
XM_011509368.1:c.*76C>A	XP_011507670.1:n.*76C>A
XM_011509369.1:c.*76C>A	XP_011507671.1:n.*76C>A
XM_011509369.2:c.*76C>A	XP_011507671.1:n.*76C>A
XM_017000851.1:c.*76C>A	XP_016856340.1:n.*76C>A
XM_017000852.1:c.*76C>A	XP_016856341.1:n.*76C>A
NM_201253.3:c.*76C>A MANE Select	NP_957705.1:n.*76C>A
NM_001193640.2:c.*76C>A	NP_001180569.1:n.*76C>A
NM_001257965.2:c.*76C>A	NP_001244894.1:n.*76C>A
NR_047563.2:n.4250C>A
NR_047564.2:n.4700C>A
NM_001257966.2:c.*76C>A	NP_001244895.1:n.*76C>A