Canonical Allele Identifier: CA344030307

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390265G>T (hg19) ; chr1:g.197421135G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421135G>T , CM000663.2:g.197421135G>T	GRCh38
NC_000001.10:g.197390265G>T , CM000663.1:g.197390265G>T	GRCh37
NC_000001.9:g.195656888G>T	NCBI36
NG_008483.1:g.157858G>T
NG_008483.2:g.224674G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1307G>T MANE Select	ENSP00000356370.3:p.Arg436Met
ENST00000638467.1:c.1307G>T	ENSP00000491102.1:p.Arg436Met
ENST00000681519.1:c.188G>T	ENSP00000505267.1:p.Arg63Met
ENST00000367397.1:c.-551G>T	ENSP00000356367.1:n.-551G>T
ENST00000367399.6:c.971G>T	ENSP00000356369.2:p.Arg324Met
ENST00000367400.7:c.1307G>T	ENSP00000356370.3:p.Arg436Met
ENST00000476483.1:n.267G>T
ENST00000484075.5:c.1307G>T	ENSP00000433932.1:p.Arg436Met
ENST00000535699.5:c.1100G>T	ENSP00000438786.1:p.Arg367Met
ENST00000538660.5:c.1307G>T	ENSP00000438091.1:p.Arg436Met
NM_001193640.1:c.971G>T	NP_001180569.1:p.Arg324Met
NM_001257965.1:c.1100G>T	NP_001244894.1:p.Arg367Met
NM_001257966.1:c.1307G>T	NP_001244895.1:p.Arg436Met
NM_201253.2:c.1307G>T	NP_957705.1:p.Arg436Met
NR_047563.1:n.1516G>T
NR_047564.1:n.1516G>T
XM_011509365.1:c.1307G>T	XP_011507667.1:p.Arg436Met
XM_011509366.1:c.1307G>T	XP_011507668.1:p.Arg436Met
XM_011509367.1:c.1307G>T	XP_011507669.1:p.Arg436Met
XM_011509368.1:c.725G>T	XP_011507670.1:p.Arg242Met
XM_011509369.1:c.-251G>T	XP_011507671.1:n.-251G>T
XM_011509365.2:c.1307G>T	XP_011507667.1:p.Arg436Met
XM_011509369.2:c.-251G>T	XP_011507671.1:n.-251G>T
XM_017000851.1:c.464G>T	XP_016856340.1:p.Arg155Met
XM_017000852.1:c.1307G>T	XP_016856341.1:p.Arg436Met
NM_201253.3:c.1307G>T MANE Select	NP_957705.1:p.Arg436Met
NM_001193640.2:c.971G>T	NP_001180569.1:p.Arg324Met
NM_001257965.2:c.1100G>T	NP_001244894.1:p.Arg367Met
NR_047563.2:n.1468G>T
NR_047564.2:n.1468G>T
NM_001257966.2:c.1307G>T	NP_001244895.1:p.Arg436Met