Canonical Allele Identifier: CA344032618

Gene: CRB1

Linked Data

• dbSNP Id: rs1276695150
• MyVariant Identifiers: chr1:g.197390747A>G (hg19) ; chr1:g.197421617A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421617A>G , CM000663.2:g.197421617A>G	GRCh38
NC_000001.10:g.197390747A>G , CM000663.1:g.197390747A>G	GRCh37
NC_000001.9:g.195657370A>G	NCBI36
NG_008483.1:g.158340A>G
NG_008483.2:g.225156A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1789A>G MANE Select	ENSP00000356370.3:p.Thr597Ala
ENST00000638467.1:c.1789A>G	ENSP00000491102.1:p.Thr597Ala
ENST00000681519.1:c.670A>G	ENSP00000505267.1:p.Thr224Ala
ENST00000367397.1:c.-69A>G	ENSP00000356367.1:n.-69A>G
ENST00000367399.6:c.1453A>G	ENSP00000356369.2:p.Thr485Ala
ENST00000367400.7:c.1789A>G	ENSP00000356370.3:p.Thr597Ala
ENST00000484075.5:c.1789A>G	ENSP00000433932.1:p.Thr597Ala
ENST00000535699.5:c.1582A>G	ENSP00000438786.1:p.Thr528Ala
ENST00000538660.5:c.1789A>G	ENSP00000438091.1:p.Thr597Ala
NM_001193640.1:c.1453A>G	NP_001180569.1:p.Thr485Ala
NM_001257965.1:c.1582A>G	NP_001244894.1:p.Thr528Ala
NM_001257966.1:c.1789A>G	NP_001244895.1:p.Thr597Ala
NM_201253.2:c.1789A>G	NP_957705.1:p.Thr597Ala
NR_047563.1:n.1922+76A>G
NR_047564.1:n.1998A>G
XM_011509365.1:c.1789A>G	XP_011507667.1:p.Thr597Ala
XM_011509366.1:c.1789A>G	XP_011507668.1:p.Thr597Ala
XM_011509367.1:c.1789A>G	XP_011507669.1:p.Thr597Ala
XM_011509368.1:c.1207A>G	XP_011507670.1:p.Thr403Ala
XM_011509369.1:c.232A>G	XP_011507671.1:p.Thr78Ala
XM_011509365.2:c.1789A>G	XP_011507667.1:p.Thr597Ala
XM_011509369.2:c.232A>G	XP_011507671.1:p.Thr78Ala
XM_017000851.1:c.946A>G	XP_016856340.1:p.Thr316Ala
XM_017000852.1:c.1789A>G	XP_016856341.1:p.Thr597Ala
NM_201253.3:c.1789A>G MANE Select	NP_957705.1:p.Thr597Ala
NM_001193640.2:c.1453A>G	NP_001180569.1:p.Thr485Ala
NM_001257965.2:c.1582A>G	NP_001244894.1:p.Thr528Ala
NR_047563.2:n.1874+76A>G
NR_047564.2:n.1950A>G
NM_001257966.2:c.1789A>G	NP_001244895.1:p.Thr597Ala