Canonical Allele Identifier: CA344028129

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390157A>T (hg19) ; chr1:g.197421027A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421027A>T , CM000663.2:g.197421027A>T	GRCh38
NC_000001.10:g.197390157A>T , CM000663.1:g.197390157A>T	GRCh37
NC_000001.9:g.195656780A>T	NCBI36
NG_008483.1:g.157750A>T
NG_008483.2:g.224566A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1199A>T MANE Select	ENSP00000356370.3:p.Glu400Val
ENST00000638467.1:c.1199A>T	ENSP00000491102.1:p.Glu400Val
ENST00000681519.1:c.80A>T	ENSP00000505267.1:p.Glu27Val
ENST00000367397.1:c.-659A>T	ENSP00000356367.1:n.-659A>T
ENST00000367399.6:c.863A>T	ENSP00000356369.2:p.Glu288Val
ENST00000367400.7:c.1199A>T	ENSP00000356370.3:p.Glu400Val
ENST00000476483.1:n.159A>T
ENST00000484075.5:c.1199A>T	ENSP00000433932.1:p.Glu400Val
ENST00000535699.5:c.992A>T	ENSP00000438786.1:p.Glu331Val
ENST00000538660.5:c.1199A>T	ENSP00000438091.1:p.Glu400Val
NM_001193640.1:c.863A>T	NP_001180569.1:p.Glu288Val
NM_001257965.1:c.992A>T	NP_001244894.1:p.Glu331Val
NM_001257966.1:c.1199A>T	NP_001244895.1:p.Glu400Val
NM_201253.2:c.1199A>T	NP_957705.1:p.Glu400Val
NR_047563.1:n.1408A>T
NR_047564.1:n.1408A>T
XM_011509365.1:c.1199A>T	XP_011507667.1:p.Glu400Val
XM_011509366.1:c.1199A>T	XP_011507668.1:p.Glu400Val
XM_011509367.1:c.1199A>T	XP_011507669.1:p.Glu400Val
XM_011509368.1:c.617A>T	XP_011507670.1:p.Glu206Val
XM_011509369.1:c.-359A>T	XP_011507671.1:n.-359A>T
XM_011509365.2:c.1199A>T	XP_011507667.1:p.Glu400Val
XM_011509369.2:c.-359A>T	XP_011507671.1:n.-359A>T
XM_017000851.1:c.356A>T	XP_016856340.1:p.Glu119Val
XM_017000852.1:c.1199A>T	XP_016856341.1:p.Glu400Val
NM_201253.3:c.1199A>T MANE Select	NP_957705.1:p.Glu400Val
NM_001193640.2:c.863A>T	NP_001180569.1:p.Glu288Val
NM_001257965.2:c.992A>T	NP_001244894.1:p.Glu331Val
NR_047563.2:n.1360A>T
NR_047564.2:n.1360A>T
NM_001257966.2:c.1199A>T	NP_001244895.1:p.Glu400Val