Canonical Allele Identifier: CA344040966

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197398671G>T (hg19) ; chr1:g.197429541G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429541G>T , CM000663.2:g.197429541G>T	GRCh38
NC_000001.10:g.197398671G>T , CM000663.1:g.197398671G>T	GRCh37
NC_000001.9:g.195665294G>T	NCBI36
NG_008483.1:g.166264G>T
NG_008483.2:g.233080G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2769G>T MANE Select	ENSP00000356370.3:p.Glu923Asp
ENST00000638467.1:c.2769G>T	ENSP00000491102.1:p.Glu923Asp
ENST00000681519.1:c.1650G>T	ENSP00000505267.1:p.Glu550Asp
ENST00000367397.1:c.912G>T	ENSP00000356367.1:p.Glu304Asp
ENST00000367399.6:c.2433G>T	ENSP00000356369.2:p.Glu811Asp
ENST00000367400.7:c.2769G>T	ENSP00000356370.3:p.Glu923Asp
ENST00000484075.5:c.2769G>T	ENSP00000433932.1:p.Glu923Asp
ENST00000535699.5:c.2697G>T	ENSP00000438786.1:p.Glu899Asp
ENST00000538660.5:c.2129-6059G>T	ENSP00000438091.1:n.2129-6059G>T
NM_001193640.1:c.2433G>T	NP_001180569.1:p.Glu811Asp
NM_001257965.1:c.2697G>T	NP_001244894.1:p.Glu899Asp
NM_001257966.1:c.2129-6059G>T	NP_001244895.1:n.2129-6059G>T
NM_201253.2:c.2769G>T	NP_957705.1:p.Glu923Asp
NR_047563.1:n.2770G>T
NR_047564.1:n.2978G>T
XM_011509365.1:c.2769G>T	XP_011507667.1:p.Glu923Asp
XM_011509366.1:c.2769G>T	XP_011507668.1:p.Glu923Asp
XM_011509367.1:c.2769G>T	XP_011507669.1:p.Glu923Asp
XM_011509368.1:c.2187G>T	XP_011507670.1:p.Glu729Asp
XM_011509369.1:c.1212G>T	XP_011507671.1:p.Glu404Asp
XM_011509365.2:c.2769G>T	XP_011507667.1:p.Glu923Asp
XM_011509369.2:c.1212G>T	XP_011507671.1:p.Glu404Asp
XM_017000851.1:c.1926G>T	XP_016856340.1:p.Glu642Asp
XM_017000852.1:c.2904G>T	XP_016856341.1:p.Glu968Asp
NM_201253.3:c.2769G>T MANE Select	NP_957705.1:p.Glu923Asp
NM_001193640.2:c.2433G>T	NP_001180569.1:p.Glu811Asp
NM_001257965.2:c.2697G>T	NP_001244894.1:p.Glu899Asp
NR_047563.2:n.2722G>T
NR_047564.2:n.2930G>T
NM_001257966.2:c.2129-6059G>T	NP_001244895.1:n.2129-6059G>T