Canonical Allele Identifier: CA528535513

Gene: CRB1

Linked Data

• dbSNP Id: rs1558168173
• gnomAD v2: 1-197446701-T-TG
• gnomAD v4: 1-197477571-T-TG
• MyVariant Identifiers: chr1:g.197446701_197446702insG (hg19) ; chr1:g.197477571_197477572insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477573dup , CM000663.2:g.197477573dup	GRCh38
NC_000001.10:g.197446703dup , CM000663.1:g.197446703dup	GRCh37
NC_000001.9:g.195713326dup	NCBI36
NG_008483.1:g.214296dup
NG_008483.2:g.281112dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4006-91dup MANE Select	ENSP00000356370.3:n.4006-91dup
ENST00000367399.6:c.3670-91dup	ENSP00000356369.2:n.3670-91dup
ENST00000367400.7:c.4006-91dup	ENSP00000356370.3:n.4006-91dup
ENST00000448952.1:c.149dup	ENSP00000395407.1:n.149dup
ENST00000484075.5:c.*117-91dup	ENSP00000433932.1:n.*117-91dup
ENST00000535699.5:c.3934-91dup	ENSP00000438786.1:n.3934-91dup
ENST00000538660.5:c.2398-91dup	ENSP00000438091.1:n.2398-91dup
NM_001193640.1:c.3670-91dup	NP_001180569.1:n.3670-91dup
NM_001257965.1:c.3934-91dup	NP_001244894.1:n.3934-91dup
NM_001257966.1:c.2398-91dup	NP_001244895.1:n.2398-91dup
NM_201253.2:c.4006-91dup	NP_957705.1:n.4006-91dup
NR_047563.1:n.4007-91dup
NR_047564.1:n.4457-91dup
XM_011509366.1:c.*20dup	XP_011507668.1:n.*20dup
XM_011509367.1:c.3879-91dup	XP_011507669.1:n.3879-91dup
XM_011509368.1:c.3424-91dup	XP_011507670.1:n.3424-91dup
XM_011509369.1:c.2449-91dup	XP_011507671.1:n.2449-91dup
XM_011509369.2:c.2449-91dup	XP_011507671.1:n.2449-91dup
XM_017000851.1:c.3163-91dup	XP_016856340.1:n.3163-91dup
XM_017000852.1:c.4141-91dup	XP_016856341.1:n.4141-91dup
NM_201253.3:c.4006-91dup MANE Select	NP_957705.1:n.4006-91dup
NM_001193640.2:c.3670-91dup	NP_001180569.1:n.3670-91dup
NM_001257965.2:c.3934-91dup	NP_001244894.1:n.3934-91dup
NR_047563.2:n.3959-91dup
NR_047564.2:n.4409-91dup
NM_001257966.2:c.2398-91dup	NP_001244895.1:n.2398-91dup