Canonical Allele Identifier: CA1311947

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421479C>T , CM000663.2:g.197421479C>T	GRCh38
NC_000001.10:g.197390609C>T , CM000663.1:g.197390609C>T	GRCh37
NC_000001.9:g.195657232C>T	NCBI36
NG_008483.1:g.158202C>T
NG_008483.2:g.225018C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.1651C>T MANE Select	NP_957705.1:p.Gln551Ter
ENST00000367400.8:c.1651C>T MANE Select	ENSP00000356370.3:p.Gln551Ter
NM_001193640.1:c.1315C>T	NP_001180569.1:p.Gln439Ter
NM_001193640.2:c.1315C>T	NP_001180569.1:p.Gln439Ter
NM_001257965.1:c.1444C>T	NP_001244894.1:p.Gln482Ter
NM_001257965.2:c.1444C>T	NP_001244894.1:p.Gln482Ter
NM_001257966.1:c.1651C>T	NP_001244895.1:p.Gln551Ter
NM_001257966.2:c.1651C>T	NP_001244895.1:p.Gln551Ter
NM_201253.2:c.1651C>T	NP_957705.1:p.Gln551Ter
NR_047563.1:n.1860C>T
NR_047563.2:n.1812C>T
NR_047564.1:n.1860C>T
NR_047564.2:n.1812C>T
ENST00000367397.1:c.-207C>T	ENSP00000356367.1:n.-207C>T
ENST00000367399.6:c.1315C>T	ENSP00000356369.2:p.Gln439Ter
ENST00000367400.7:c.1651C>T	ENSP00000356370.3:p.Gln551Ter
ENST00000484075.5:c.1651C>T	ENSP00000433932.1:p.Gln551Ter
ENST00000535699.5:c.1444C>T	ENSP00000438786.1:p.Gln482Ter
ENST00000538660.5:c.1651C>T	ENSP00000438091.1:p.Gln551Ter
ENST00000638467.1:c.1651C>T	ENSP00000491102.1:p.Gln551Ter
ENST00000681519.1:c.532C>T	ENSP00000505267.1:p.Gln178Ter
XM_011509365.1:c.1651C>T	XP_011507667.1:p.Gln551Ter
XM_011509365.2:c.1651C>T	XP_011507667.1:p.Gln551Ter
XM_011509366.1:c.1651C>T	XP_011507668.1:p.Gln551Ter
XM_011509367.1:c.1651C>T	XP_011507669.1:p.Gln551Ter
XM_011509368.1:c.1069C>T	XP_011507670.1:p.Gln357Ter
XM_011509369.1:c.94C>T	XP_011507671.1:p.Gln32Ter
XM_011509369.2:c.94C>T	XP_011507671.1:p.Gln32Ter
XM_017000851.1:c.808C>T	XP_016856340.1:p.Gln270Ter
XM_017000852.1:c.1651C>T	XP_016856341.1:p.Gln551Ter