Canonical Allele Identifier: CA344028290

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390175G>C (hg19) ; chr1:g.197421045G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421045G>C , CM000663.2:g.197421045G>C	GRCh38
NC_000001.10:g.197390175G>C , CM000663.1:g.197390175G>C	GRCh37
NC_000001.9:g.195656798G>C	NCBI36
NG_008483.1:g.157768G>C
NG_008483.2:g.224584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1217G>C MANE Select	ENSP00000356370.3:p.Cys406Ser
ENST00000638467.1:c.1217G>C	ENSP00000491102.1:p.Cys406Ser
ENST00000681519.1:c.98G>C	ENSP00000505267.1:p.Cys33Ser
ENST00000367397.1:c.-641G>C	ENSP00000356367.1:n.-641G>C
ENST00000367399.6:c.881G>C	ENSP00000356369.2:p.Cys294Ser
ENST00000367400.7:c.1217G>C	ENSP00000356370.3:p.Cys406Ser
ENST00000476483.1:n.177G>C
ENST00000484075.5:c.1217G>C	ENSP00000433932.1:p.Cys406Ser
ENST00000535699.5:c.1010G>C	ENSP00000438786.1:p.Cys337Ser
ENST00000538660.5:c.1217G>C	ENSP00000438091.1:p.Cys406Ser
NM_001193640.1:c.881G>C	NP_001180569.1:p.Cys294Ser
NM_001257965.1:c.1010G>C	NP_001244894.1:p.Cys337Ser
NM_001257966.1:c.1217G>C	NP_001244895.1:p.Cys406Ser
NM_201253.2:c.1217G>C	NP_957705.1:p.Cys406Ser
NR_047563.1:n.1426G>C
NR_047564.1:n.1426G>C
XM_011509365.1:c.1217G>C	XP_011507667.1:p.Cys406Ser
XM_011509366.1:c.1217G>C	XP_011507668.1:p.Cys406Ser
XM_011509367.1:c.1217G>C	XP_011507669.1:p.Cys406Ser
XM_011509368.1:c.635G>C	XP_011507670.1:p.Cys212Ser
XM_011509369.1:c.-341G>C	XP_011507671.1:n.-341G>C
XM_011509365.2:c.1217G>C	XP_011507667.1:p.Cys406Ser
XM_011509369.2:c.-341G>C	XP_011507671.1:n.-341G>C
XM_017000851.1:c.374G>C	XP_016856340.1:p.Cys125Ser
XM_017000852.1:c.1217G>C	XP_016856341.1:p.Cys406Ser
NM_201253.3:c.1217G>C MANE Select	NP_957705.1:p.Cys406Ser
NM_001193640.2:c.881G>C	NP_001180569.1:p.Cys294Ser
NM_001257965.2:c.1010G>C	NP_001244894.1:p.Cys337Ser
NR_047563.2:n.1378G>C
NR_047564.2:n.1378G>C
NM_001257966.2:c.1217G>C	NP_001244895.1:p.Cys406Ser