Canonical Allele Identifier: CA344030972

Gene: CRB1

Linked Data

• dbSNP Id: rs1664297379
• COSMIC: COSM4674579 ; COSM4674580
• MyVariant Identifiers: chr1:g.197390411A>G (hg19) ; chr1:g.197421281A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421281A>G , CM000663.2:g.197421281A>G	GRCh38
NC_000001.10:g.197390411A>G , CM000663.1:g.197390411A>G	GRCh37
NC_000001.9:g.195657034A>G	NCBI36
NG_008483.1:g.158004A>G
NG_008483.2:g.224820A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1453A>G MANE Select	ENSP00000356370.3:p.Thr485Ala
ENST00000638467.1:c.1453A>G	ENSP00000491102.1:p.Thr485Ala
ENST00000681519.1:c.334A>G	ENSP00000505267.1:p.Thr112Ala
ENST00000367397.1:c.-405A>G	ENSP00000356367.1:n.-405A>G
ENST00000367399.6:c.1117A>G	ENSP00000356369.2:p.Thr373Ala
ENST00000367400.7:c.1453A>G	ENSP00000356370.3:p.Thr485Ala
ENST00000476483.1:n.413A>G
ENST00000484075.5:c.1453A>G	ENSP00000433932.1:p.Thr485Ala
ENST00000535699.5:c.1246A>G	ENSP00000438786.1:p.Thr416Ala
ENST00000538660.5:c.1453A>G	ENSP00000438091.1:p.Thr485Ala
NM_001193640.1:c.1117A>G	NP_001180569.1:p.Thr373Ala
NM_001257965.1:c.1246A>G	NP_001244894.1:p.Thr416Ala
NM_001257966.1:c.1453A>G	NP_001244895.1:p.Thr485Ala
NM_201253.2:c.1453A>G	NP_957705.1:p.Thr485Ala
NR_047563.1:n.1662A>G
NR_047564.1:n.1662A>G
XM_011509365.1:c.1453A>G	XP_011507667.1:p.Thr485Ala
XM_011509366.1:c.1453A>G	XP_011507668.1:p.Thr485Ala
XM_011509367.1:c.1453A>G	XP_011507669.1:p.Thr485Ala
XM_011509368.1:c.871A>G	XP_011507670.1:p.Thr291Ala
XM_011509369.1:c.-105A>G	XP_011507671.1:n.-105A>G
XM_011509365.2:c.1453A>G	XP_011507667.1:p.Thr485Ala
XM_011509369.2:c.-105A>G	XP_011507671.1:n.-105A>G
XM_017000851.1:c.610A>G	XP_016856340.1:p.Thr204Ala
XM_017000852.1:c.1453A>G	XP_016856341.1:p.Thr485Ala
NM_201253.3:c.1453A>G MANE Select	NP_957705.1:p.Thr485Ala
NM_001193640.2:c.1117A>G	NP_001180569.1:p.Thr373Ala
NM_001257965.2:c.1246A>G	NP_001244894.1:p.Thr416Ala
NR_047563.2:n.1614A>G
NR_047564.2:n.1614A>G
NM_001257966.2:c.1453A>G	NP_001244895.1:p.Thr485Ala