Canonical Allele Identifier: CA344043487
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197434777G>A , CM000663.2:g.197434777G>A GRCh38
NC_000001.10:g.197403907G>A , CM000663.1:g.197403907G>A GRCh37
NC_000001.9:g.195670530G>A NCBI36
NG_008483.1:g.171500G>A
NG_008483.2:g.238316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2914G>A MANE Select ENSP00000356370.3:p.Glu972Lys
ENST00000638467.1:c.2914G>A ENSP00000491102.1:p.Glu972Lys
ENST00000681519.1:c.1795G>A ENSP00000505267.1:p.Glu599Lys
ENST00000367397.1:c.1057G>A ENSP00000356367.1:p.Glu353Lys
ENST00000367399.6:c.2578G>A ENSP00000356369.2:p.Glu860Lys
ENST00000367400.7:c.2914G>A ENSP00000356370.3:p.Glu972Lys
ENST00000484075.5:c.2914G>A ENSP00000433932.1:p.Glu972Lys
ENST00000535699.5:c.2842G>A ENSP00000438786.1:p.Glu948Lys
ENST00000538660.5:c.2129-823G>A ENSP00000438091.1:n.2129-823G>A
NM_001193640.1:c.2578G>A NP_001180569.1:p.Glu860Lys
NM_001257965.1:c.2842G>A NP_001244894.1:p.Glu948Lys
NM_001257966.1:c.2129-823G>A NP_001244895.1:n.2129-823G>A
NM_201253.2:c.2914G>A NP_957705.1:p.Glu972Lys
NR_047563.1:n.2915G>A
NR_047564.1:n.3123G>A
XM_011509365.1:c.2914G>A XP_011507667.1:p.Glu972Lys
XM_011509366.1:c.2914G>A XP_011507668.1:p.Glu972Lys
XM_011509367.1:c.2914G>A XP_011507669.1:p.Glu972Lys
XM_011509368.1:c.2332G>A XP_011507670.1:p.Glu778Lys
XM_011509369.1:c.1357G>A XP_011507671.1:p.Glu453Lys
XM_011509365.2:c.2914G>A XP_011507667.1:p.Glu972Lys
XM_011509369.2:c.1357G>A XP_011507671.1:p.Glu453Lys
XM_017000851.1:c.2071G>A XP_016856340.1:p.Glu691Lys
XM_017000852.1:c.3049G>A XP_016856341.1:p.Glu1017Lys
NM_201253.3:c.2914G>A MANE Select NP_957705.1:p.Glu972Lys
NM_001193640.2:c.2578G>A NP_001180569.1:p.Glu860Lys
NM_001257965.2:c.2842G>A NP_001244894.1:p.Glu948Lys
NR_047563.2:n.2867G>A
NR_047564.2:n.3075G>A
NM_001257966.2:c.2129-823G>A NP_001244895.1:n.2129-823G>A