Canonical Allele Identifier: CA1218063132

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421449T= , CM000663.2:g.197421449T=	GRCh38
NC_000001.10:g.197390579T= , CM000663.1:g.197390579T=	GRCh37
NC_000001.9:g.195657202T=	NCBI36
NG_008483.1:g.158172T=
NG_008483.2:g.224988T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1621T= MANE Select	ENSP00000356370.3:p.Tyr541=
ENST00000638467.1:c.1621T=	ENSP00000491102.1:p.Tyr541=
ENST00000681519.1:c.502T=	ENSP00000505267.1:p.Tyr168=
ENST00000367397.1:c.-237T=	ENSP00000356367.1:n.-237T=
ENST00000367399.6:c.1285T=	ENSP00000356369.2:p.Tyr429=
ENST00000367400.7:c.1621T=	ENSP00000356370.3:p.Tyr541=
ENST00000484075.5:c.1621T=	ENSP00000433932.1:p.Tyr541=
ENST00000535699.5:c.1414T=	ENSP00000438786.1:p.Tyr472=
ENST00000538660.5:c.1621T=	ENSP00000438091.1:p.Tyr541=
NM_001193640.1:c.1285T=	NP_001180569.1:p.Tyr429=
NM_001257965.1:c.1414T=	NP_001244894.1:p.Tyr472=
NM_001257966.1:c.1621T=	NP_001244895.1:p.Tyr541=
NM_201253.2:c.1621T=	NP_957705.1:p.Tyr541=
NR_047563.1:n.1830T=
NR_047564.1:n.1830T=
XM_011509365.1:c.1621T=	XP_011507667.1:p.Tyr541=
XM_011509366.1:c.1621T=	XP_011507668.1:p.Tyr541=
XM_011509367.1:c.1621T=	XP_011507669.1:p.Tyr541=
XM_011509368.1:c.1039T=	XP_011507670.1:p.Tyr347=
XM_011509369.1:c.64T=	XP_011507671.1:p.Tyr22=
XM_011509365.2:c.1621T=	XP_011507667.1:p.Tyr541=
XM_011509369.2:c.64T=	XP_011507671.1:p.Tyr22=
XM_017000851.1:c.778T=	XP_016856340.1:p.Tyr260=
XM_017000852.1:c.1621T=	XP_016856341.1:p.Tyr541=
NM_201253.3:c.1621T= MANE Select	NP_957705.1:p.Tyr541=
NM_001193640.2:c.1285T=	NP_001180569.1:p.Tyr429=
NM_001257965.2:c.1414T=	NP_001244894.1:p.Tyr472=
NR_047563.2:n.1782T=
NR_047564.2:n.1782T=
NM_001257966.2:c.1621T=	NP_001244895.1:p.Tyr541=