Canonical Allele Identifier: CA344031517

Gene: CRB1

Linked Data

• gnomAD v4: 1-197421399-T-G
• MyVariant Identifiers: chr1:g.197390529T>G (hg19) ; chr1:g.197421399T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421399T>G , CM000663.2:g.197421399T>G	GRCh38
NC_000001.10:g.197390529T>G , CM000663.1:g.197390529T>G	GRCh37
NC_000001.9:g.195657152T>G	NCBI36
NG_008483.1:g.158122T>G
NG_008483.2:g.224938T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1571T>G MANE Select	ENSP00000356370.3:p.Leu524Arg
ENST00000638467.1:c.1571T>G	ENSP00000491102.1:p.Leu524Arg
ENST00000681519.1:c.452T>G	ENSP00000505267.1:p.Leu151Arg
ENST00000367397.1:c.-287T>G	ENSP00000356367.1:n.-287T>G
ENST00000367399.6:c.1235T>G	ENSP00000356369.2:p.Leu412Arg
ENST00000367400.7:c.1571T>G	ENSP00000356370.3:p.Leu524Arg
ENST00000476483.1:n.531T>G
ENST00000484075.5:c.1571T>G	ENSP00000433932.1:p.Leu524Arg
ENST00000535699.5:c.1364T>G	ENSP00000438786.1:p.Leu455Arg
ENST00000538660.5:c.1571T>G	ENSP00000438091.1:p.Leu524Arg
NM_001193640.1:c.1235T>G	NP_001180569.1:p.Leu412Arg
NM_001257965.1:c.1364T>G	NP_001244894.1:p.Leu455Arg
NM_001257966.1:c.1571T>G	NP_001244895.1:p.Leu524Arg
NM_201253.2:c.1571T>G	NP_957705.1:p.Leu524Arg
NR_047563.1:n.1780T>G
NR_047564.1:n.1780T>G
XM_011509365.1:c.1571T>G	XP_011507667.1:p.Leu524Arg
XM_011509366.1:c.1571T>G	XP_011507668.1:p.Leu524Arg
XM_011509367.1:c.1571T>G	XP_011507669.1:p.Leu524Arg
XM_011509368.1:c.989T>G	XP_011507670.1:p.Leu330Arg
XM_011509369.1:c.14T>G	XP_011507671.1:p.Leu5Arg
XM_011509365.2:c.1571T>G	XP_011507667.1:p.Leu524Arg
XM_011509369.2:c.14T>G	XP_011507671.1:p.Leu5Arg
XM_017000851.1:c.728T>G	XP_016856340.1:p.Leu243Arg
XM_017000852.1:c.1571T>G	XP_016856341.1:p.Leu524Arg
NM_201253.3:c.1571T>G MANE Select	NP_957705.1:p.Leu524Arg
NM_001193640.2:c.1235T>G	NP_001180569.1:p.Leu412Arg
NM_001257965.2:c.1364T>G	NP_001244894.1:p.Leu455Arg
NR_047563.2:n.1732T>G
NR_047564.2:n.1732T>G
NM_001257966.2:c.1571T>G	NP_001244895.1:p.Leu524Arg