Canonical Allele Identifier: CA344035443

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446815G>C (hg19) ; chr1:g.197477685G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477685G>C , CM000663.2:g.197477685G>C	GRCh38
NC_000001.10:g.197446815G>C , CM000663.1:g.197446815G>C	GRCh37
NC_000001.9:g.195713438G>C	NCBI36
NG_008483.1:g.214408G>C
NG_008483.2:g.281224G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4027G>C MANE Select	ENSP00000356370.3:p.Asp1343His
ENST00000367399.6:c.3691G>C	ENSP00000356369.2:p.Asp1231His
ENST00000367400.7:c.4027G>C	ENSP00000356370.3:p.Asp1343His
ENST00000448952.1:c.261G>C	ENSP00000395407.1:n.261G>C
ENST00000484075.5:c.*138G>C	ENSP00000433932.1:n.*138G>C
ENST00000535699.5:c.3955G>C	ENSP00000438786.1:p.Asp1319His
ENST00000538660.5:c.2419G>C	ENSP00000438091.1:p.Asp807His
NM_001193640.1:c.3691G>C	NP_001180569.1:p.Asp1231His
NM_001257965.1:c.3955G>C	NP_001244894.1:p.Asp1319His
NM_001257966.1:c.2419G>C	NP_001244895.1:p.Asp807His
NM_201253.2:c.4027G>C	NP_957705.1:p.Asp1343His
NR_047563.1:n.4028G>C
NR_047564.1:n.4478G>C
XM_011509366.1:c.*132G>C	XP_011507668.1:n.*132G>C
XM_011509367.1:c.*6G>C	XP_011507669.1:n.*6G>C
XM_011509368.1:c.3445G>C	XP_011507670.1:p.Asp1149His
XM_011509369.1:c.2470G>C	XP_011507671.1:p.Asp824His
XM_011509369.2:c.2470G>C	XP_011507671.1:p.Asp824His
XM_017000851.1:c.3184G>C	XP_016856340.1:p.Asp1062His
XM_017000852.1:c.4162G>C	XP_016856341.1:p.Asp1388His
NM_201253.3:c.4027G>C MANE Select	NP_957705.1:p.Asp1343His
NM_001193640.2:c.3691G>C	NP_001180569.1:p.Asp1231His
NM_001257965.2:c.3955G>C	NP_001244894.1:p.Asp1319His
NR_047563.2:n.3980G>C
NR_047564.2:n.4430G>C
NM_001257966.2:c.2419G>C	NP_001244895.1:p.Asp807His