Canonical Allele Identifier: CA344033660

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421863C>T , CM000663.2:g.197421863C>T	GRCh38
NC_000001.10:g.197390993C>T , CM000663.1:g.197390993C>T	GRCh37
NC_000001.9:g.195657616C>T	NCBI36
NG_008483.1:g.158586C>T
NG_008483.2:g.225402C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.2035C>T MANE Select	NP_957705.1:p.Gln679Ter
ENST00000367400.8:c.2035C>T MANE Select	ENSP00000356370.3:p.Gln679Ter
NM_001193640.1:c.1699C>T	NP_001180569.1:p.Gln567Ter
NM_001193640.2:c.1699C>T	NP_001180569.1:p.Gln567Ter
NM_001257965.1:c.1828C>T	NP_001244894.1:p.Gln610Ter
NM_001257965.2:c.1828C>T	NP_001244894.1:p.Gln610Ter
NM_001257966.1:c.2035C>T	NP_001244895.1:p.Gln679Ter
NM_001257966.2:c.2035C>T	NP_001244895.1:p.Gln679Ter
NM_201253.2:c.2035C>T	NP_957705.1:p.Gln679Ter
NR_047563.1:n.2036C>T
NR_047563.2:n.1988C>T
NR_047564.1:n.2244C>T
NR_047564.2:n.2196C>T
ENST00000367397.1:c.178C>T	ENSP00000356367.1:p.Gln60Ter
ENST00000367399.6:c.1699C>T	ENSP00000356369.2:p.Gln567Ter
ENST00000367400.7:c.2035C>T	ENSP00000356370.3:p.Gln679Ter
ENST00000484075.5:c.2035C>T	ENSP00000433932.1:p.Gln679Ter
ENST00000535699.5:c.1828C>T	ENSP00000438786.1:p.Gln610Ter
ENST00000538660.5:c.2035C>T	ENSP00000438091.1:p.Gln679Ter
ENST00000638467.1:c.2035C>T	ENSP00000491102.1:p.Gln679Ter
ENST00000681519.1:c.916C>T	ENSP00000505267.1:p.Gln306Ter
XM_011509365.1:c.2035C>T	XP_011507667.1:p.Gln679Ter
XM_011509365.2:c.2035C>T	XP_011507667.1:p.Gln679Ter
XM_011509366.1:c.2035C>T	XP_011507668.1:p.Gln679Ter
XM_011509367.1:c.2035C>T	XP_011507669.1:p.Gln679Ter
XM_011509368.1:c.1453C>T	XP_011507670.1:p.Gln485Ter
XM_011509369.1:c.478C>T	XP_011507671.1:p.Gln160Ter
XM_011509369.2:c.478C>T	XP_011507671.1:p.Gln160Ter
XM_017000851.1:c.1192C>T	XP_016856340.1:p.Gln398Ter
XM_017000852.1:c.2035C>T	XP_016856341.1:p.Gln679Ter