Canonical Allele Identifier: CA344047539

Gene: CRB1

Linked Data

• dbSNP Id: rs1665091270
• MyVariant Identifiers: chr1:g.197404381A>G (hg19) ; chr1:g.197435251A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435251A>G , CM000663.2:g.197435251A>G	GRCh38
NC_000001.10:g.197404381A>G , CM000663.1:g.197404381A>G	GRCh37
NC_000001.9:g.195671004A>G	NCBI36
NG_008483.1:g.171974A>G
NG_008483.2:g.238790A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3388A>G MANE Select	ENSP00000356370.3:p.Thr1130Ala
ENST00000638467.1:c.3388A>G	ENSP00000491102.1:p.Thr1130Ala
ENST00000681519.1:c.2269A>G	ENSP00000505267.1:p.Thr757Ala
ENST00000367397.1:c.1531A>G	ENSP00000356367.1:p.Thr511Ala
ENST00000367399.6:c.3052A>G	ENSP00000356369.2:p.Thr1018Ala
ENST00000367400.7:c.3388A>G	ENSP00000356370.3:p.Thr1130Ala
ENST00000484075.5:c.3388A>G	ENSP00000433932.1:p.Thr1130Ala
ENST00000535699.5:c.3316A>G	ENSP00000438786.1:p.Thr1106Ala
ENST00000538660.5:c.2129-349A>G	ENSP00000438091.1:n.2129-349A>G
NM_001193640.1:c.3052A>G	NP_001180569.1:p.Thr1018Ala
NM_001257965.1:c.3316A>G	NP_001244894.1:p.Thr1106Ala
NM_001257966.1:c.2129-349A>G	NP_001244895.1:n.2129-349A>G
NM_201253.2:c.3388A>G	NP_957705.1:p.Thr1130Ala
NR_047563.1:n.3389A>G
NR_047564.1:n.3597A>G
XM_011509365.1:c.3388A>G	XP_011507667.1:p.Thr1130Ala
XM_011509366.1:c.3388A>G	XP_011507668.1:p.Thr1130Ala
XM_011509367.1:c.3388A>G	XP_011507669.1:p.Thr1130Ala
XM_011509368.1:c.2806A>G	XP_011507670.1:p.Thr936Ala
XM_011509369.1:c.1831A>G	XP_011507671.1:p.Thr611Ala
XM_011509365.2:c.3388A>G	XP_011507667.1:p.Thr1130Ala
XM_011509369.2:c.1831A>G	XP_011507671.1:p.Thr611Ala
XM_017000851.1:c.2545A>G	XP_016856340.1:p.Thr849Ala
XM_017000852.1:c.3523A>G	XP_016856341.1:p.Thr1175Ala
NM_201253.3:c.3388A>G MANE Select	NP_957705.1:p.Thr1130Ala
NM_001193640.2:c.3052A>G	NP_001180569.1:p.Thr1018Ala
NM_001257965.2:c.3316A>G	NP_001244894.1:p.Thr1106Ala
NR_047563.2:n.3341A>G
NR_047564.2:n.3549A>G
NM_001257966.2:c.2129-349A>G	NP_001244895.1:n.2129-349A>G