Canonical Allele Identifier: CA1218068722

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434927A= , CM000663.2:g.197434927A=	GRCh38
NC_000001.10:g.197404057A= , CM000663.1:g.197404057A=	GRCh37
NC_000001.9:g.195670680A=	NCBI36
NG_008483.1:g.171650A=
NG_008483.2:g.238466A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3064A= MANE Select	ENSP00000356370.3:p.Ser1022=
ENST00000638467.1:c.3064A=	ENSP00000491102.1:p.Ser1022=
ENST00000681519.1:c.1945A=	ENSP00000505267.1:p.Ser649=
ENST00000367397.1:c.1207A=	ENSP00000356367.1:p.Ser403=
ENST00000367399.6:c.2728A=	ENSP00000356369.2:p.Ser910=
ENST00000367400.7:c.3064A=	ENSP00000356370.3:p.Ser1022=
ENST00000484075.5:c.3064A=	ENSP00000433932.1:p.Ser1022=
ENST00000535699.5:c.2992A=	ENSP00000438786.1:p.Ser998=
ENST00000538660.5:c.2129-673A=	ENSP00000438091.1:n.2129-673A=
NM_001193640.1:c.2728A=	NP_001180569.1:p.Ser910=
NM_001257965.1:c.2992A=	NP_001244894.1:p.Ser998=
NM_001257966.1:c.2129-673A=	NP_001244895.1:n.2129-673A=
NM_201253.2:c.3064A=	NP_957705.1:p.Ser1022=
NR_047563.1:n.3065A=
NR_047564.1:n.3273A=
XM_011509365.1:c.3064A=	XP_011507667.1:p.Ser1022=
XM_011509366.1:c.3064A=	XP_011507668.1:p.Ser1022=
XM_011509367.1:c.3064A=	XP_011507669.1:p.Ser1022=
XM_011509368.1:c.2482A=	XP_011507670.1:p.Ser828=
XM_011509369.1:c.1507A=	XP_011507671.1:p.Ser503=
XM_011509365.2:c.3064A=	XP_011507667.1:p.Ser1022=
XM_011509369.2:c.1507A=	XP_011507671.1:p.Ser503=
XM_017000851.1:c.2221A=	XP_016856340.1:p.Ser741=
XM_017000852.1:c.3199A=	XP_016856341.1:p.Ser1067=
NM_201253.3:c.3064A= MANE Select	NP_957705.1:p.Ser1022=
NM_001193640.2:c.2728A=	NP_001180569.1:p.Ser910=
NM_001257965.2:c.2992A=	NP_001244894.1:p.Ser998=
NR_047563.2:n.3017A=
NR_047564.2:n.3225A=
NM_001257966.2:c.2129-673A=	NP_001244895.1:n.2129-673A=