Canonical Allele Identifier: CA422808201

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390278T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421148T>C , CM000663.2:g.197421148T>C	GRCh38
NC_000001.10:g.197390278T>C , CM000663.1:g.197390278T>C	GRCh37
NC_000001.9:g.195656901T>C	NCBI36
NG_008483.1:g.157871T>C
NG_008483.2:g.224687T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1320T>C MANE Select	ENSP00000356370.3:p.Asp440=
ENST00000638467.1:c.1320T>C	ENSP00000491102.1:p.Asp440=
ENST00000681519.1:c.201T>C	ENSP00000505267.1:p.Asp67=
ENST00000367397.1:c.-538T>C	ENSP00000356367.1:n.-538T>C
ENST00000367399.6:c.984T>C	ENSP00000356369.2:p.Asp328=
ENST00000367400.7:c.1320T>C	ENSP00000356370.3:p.Asp440=
ENST00000476483.1:n.280T>C
ENST00000484075.5:c.1320T>C	ENSP00000433932.1:p.Asp440=
ENST00000535699.5:c.1113T>C	ENSP00000438786.1:p.Asp371=
ENST00000538660.5:c.1320T>C	ENSP00000438091.1:p.Asp440=
NM_001193640.1:c.984T>C	NP_001180569.1:p.Asp328=
NM_001257965.1:c.1113T>C	NP_001244894.1:p.Asp371=
NM_001257966.1:c.1320T>C	NP_001244895.1:p.Asp440=
NM_201253.2:c.1320T>C	NP_957705.1:p.Asp440=
NR_047563.1:n.1529T>C
NR_047564.1:n.1529T>C
XM_011509365.1:c.1320T>C	XP_011507667.1:p.Asp440=
XM_011509366.1:c.1320T>C	XP_011507668.1:p.Asp440=
XM_011509367.1:c.1320T>C	XP_011507669.1:p.Asp440=
XM_011509368.1:c.738T>C	XP_011507670.1:p.Asp246=
XM_011509369.1:c.-238T>C	XP_011507671.1:n.-238T>C
XM_011509365.2:c.1320T>C	XP_011507667.1:p.Asp440=
XM_011509369.2:c.-238T>C	XP_011507671.1:n.-238T>C
XM_017000851.1:c.477T>C	XP_016856340.1:p.Asp159=
XM_017000852.1:c.1320T>C	XP_016856341.1:p.Asp440=
NM_201253.3:c.1320T>C MANE Select	NP_957705.1:p.Asp440=
NM_001193640.2:c.984T>C	NP_001180569.1:p.Asp328=
NM_001257965.2:c.1113T>C	NP_001244894.1:p.Asp371=
NR_047563.2:n.1481T>C
NR_047564.2:n.1481T>C
NM_001257966.2:c.1320T>C	NP_001244895.1:p.Asp440=