Canonical Allele Identifier: CA344044237

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403972A>C (hg19) ; chr1:g.197434842A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434842A>C , CM000663.2:g.197434842A>C	GRCh38
NC_000001.10:g.197403972A>C , CM000663.1:g.197403972A>C	GRCh37
NC_000001.9:g.195670595A>C	NCBI36
NG_008483.1:g.171565A>C
NG_008483.2:g.238381A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2979A>C MANE Select	ENSP00000356370.3:p.Glu993Asp
ENST00000638467.1:c.2979A>C	ENSP00000491102.1:p.Glu993Asp
ENST00000681519.1:c.1860A>C	ENSP00000505267.1:p.Glu620Asp
ENST00000367397.1:c.1122A>C	ENSP00000356367.1:p.Glu374Asp
ENST00000367399.6:c.2643A>C	ENSP00000356369.2:p.Glu881Asp
ENST00000367400.7:c.2979A>C	ENSP00000356370.3:p.Glu993Asp
ENST00000484075.5:c.2979A>C	ENSP00000433932.1:p.Glu993Asp
ENST00000535699.5:c.2907A>C	ENSP00000438786.1:p.Glu969Asp
ENST00000538660.5:c.2129-758A>C	ENSP00000438091.1:n.2129-758A>C
NM_001193640.1:c.2643A>C	NP_001180569.1:p.Glu881Asp
NM_001257965.1:c.2907A>C	NP_001244894.1:p.Glu969Asp
NM_001257966.1:c.2129-758A>C	NP_001244895.1:n.2129-758A>C
NM_201253.2:c.2979A>C	NP_957705.1:p.Glu993Asp
NR_047563.1:n.2980A>C
NR_047564.1:n.3188A>C
XM_011509365.1:c.2979A>C	XP_011507667.1:p.Glu993Asp
XM_011509366.1:c.2979A>C	XP_011507668.1:p.Glu993Asp
XM_011509367.1:c.2979A>C	XP_011507669.1:p.Glu993Asp
XM_011509368.1:c.2397A>C	XP_011507670.1:p.Glu799Asp
XM_011509369.1:c.1422A>C	XP_011507671.1:p.Glu474Asp
XM_011509365.2:c.2979A>C	XP_011507667.1:p.Glu993Asp
XM_011509369.2:c.1422A>C	XP_011507671.1:p.Glu474Asp
XM_017000851.1:c.2136A>C	XP_016856340.1:p.Glu712Asp
XM_017000852.1:c.3114A>C	XP_016856341.1:p.Glu1038Asp
NM_201253.3:c.2979A>C MANE Select	NP_957705.1:p.Glu993Asp
NM_001193640.2:c.2643A>C	NP_001180569.1:p.Glu881Asp
NM_001257965.2:c.2907A>C	NP_001244894.1:p.Glu969Asp
NR_047563.2:n.2932A>C
NR_047564.2:n.3140A>C
NM_001257966.2:c.2129-758A>C	NP_001244895.1:n.2129-758A>C