Canonical Allele Identifier: CA344030055

Gene: CRB1

Linked Data

• gnomAD v4: 1-197421092-C-T
• COSMIC: COSM6060707 ; COSM6060708
• MyVariant Identifiers: chr1:g.197390222C>T (hg19) ; chr1:g.197421092C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421092C>T , CM000663.2:g.197421092C>T	GRCh38
NC_000001.10:g.197390222C>T , CM000663.1:g.197390222C>T	GRCh37
NC_000001.9:g.195656845C>T	NCBI36
NG_008483.1:g.157815C>T
NG_008483.2:g.224631C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1264C>T MANE Select	ENSP00000356370.3:p.His422Tyr
ENST00000638467.1:c.1264C>T	ENSP00000491102.1:p.His422Tyr
ENST00000681519.1:c.145C>T	ENSP00000505267.1:p.His49Tyr
ENST00000367397.1:c.-594C>T	ENSP00000356367.1:n.-594C>T
ENST00000367399.6:c.928C>T	ENSP00000356369.2:p.His310Tyr
ENST00000367400.7:c.1264C>T	ENSP00000356370.3:p.His422Tyr
ENST00000476483.1:n.224C>T
ENST00000484075.5:c.1264C>T	ENSP00000433932.1:p.His422Tyr
ENST00000535699.5:c.1057C>T	ENSP00000438786.1:p.His353Tyr
ENST00000538660.5:c.1264C>T	ENSP00000438091.1:p.His422Tyr
NM_001193640.1:c.928C>T	NP_001180569.1:p.His310Tyr
NM_001257965.1:c.1057C>T	NP_001244894.1:p.His353Tyr
NM_001257966.1:c.1264C>T	NP_001244895.1:p.His422Tyr
NM_201253.2:c.1264C>T	NP_957705.1:p.His422Tyr
NR_047563.1:n.1473C>T
NR_047564.1:n.1473C>T
XM_011509365.1:c.1264C>T	XP_011507667.1:p.His422Tyr
XM_011509366.1:c.1264C>T	XP_011507668.1:p.His422Tyr
XM_011509367.1:c.1264C>T	XP_011507669.1:p.His422Tyr
XM_011509368.1:c.682C>T	XP_011507670.1:p.His228Tyr
XM_011509369.1:c.-294C>T	XP_011507671.1:n.-294C>T
XM_011509365.2:c.1264C>T	XP_011507667.1:p.His422Tyr
XM_011509369.2:c.-294C>T	XP_011507671.1:n.-294C>T
XM_017000851.1:c.421C>T	XP_016856340.1:p.His141Tyr
XM_017000852.1:c.1264C>T	XP_016856341.1:p.His422Tyr
NM_201253.3:c.1264C>T MANE Select	NP_957705.1:p.His422Tyr
NM_001193640.2:c.928C>T	NP_001180569.1:p.His310Tyr
NM_001257965.2:c.1057C>T	NP_001244894.1:p.His353Tyr
NR_047563.2:n.1425C>T
NR_047564.2:n.1425C>T
NM_001257966.2:c.1264C>T	NP_001244895.1:p.His422Tyr