Canonical Allele Identifier: CA344031185

Gene: CRB1

Linked Data

• gnomAD v4: 1-197421326-T-A
• MyVariant Identifiers: chr1:g.197390456T>A (hg19) ; chr1:g.197421326T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421326T>A , CM000663.2:g.197421326T>A	GRCh38
NC_000001.10:g.197390456T>A , CM000663.1:g.197390456T>A	GRCh37
NC_000001.9:g.195657079T>A	NCBI36
NG_008483.1:g.158049T>A
NG_008483.2:g.224865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1498T>A MANE Select	ENSP00000356370.3:p.Ser500Thr
ENST00000638467.1:c.1498T>A	ENSP00000491102.1:p.Ser500Thr
ENST00000681519.1:c.379T>A	ENSP00000505267.1:p.Ser127Thr
ENST00000367397.1:c.-360T>A	ENSP00000356367.1:n.-360T>A
ENST00000367399.6:c.1162T>A	ENSP00000356369.2:p.Ser388Thr
ENST00000367400.7:c.1498T>A	ENSP00000356370.3:p.Ser500Thr
ENST00000476483.1:n.458T>A
ENST00000484075.5:c.1498T>A	ENSP00000433932.1:p.Ser500Thr
ENST00000535699.5:c.1291T>A	ENSP00000438786.1:p.Ser431Thr
ENST00000538660.5:c.1498T>A	ENSP00000438091.1:p.Ser500Thr
NM_001193640.1:c.1162T>A	NP_001180569.1:p.Ser388Thr
NM_001257965.1:c.1291T>A	NP_001244894.1:p.Ser431Thr
NM_001257966.1:c.1498T>A	NP_001244895.1:p.Ser500Thr
NM_201253.2:c.1498T>A	NP_957705.1:p.Ser500Thr
NR_047563.1:n.1707T>A
NR_047564.1:n.1707T>A
XM_011509365.1:c.1498T>A	XP_011507667.1:p.Ser500Thr
XM_011509366.1:c.1498T>A	XP_011507668.1:p.Ser500Thr
XM_011509367.1:c.1498T>A	XP_011507669.1:p.Ser500Thr
XM_011509368.1:c.916T>A	XP_011507670.1:p.Ser306Thr
XM_011509369.1:c.-60T>A	XP_011507671.1:n.-60T>A
XM_011509365.2:c.1498T>A	XP_011507667.1:p.Ser500Thr
XM_011509369.2:c.-60T>A	XP_011507671.1:n.-60T>A
XM_017000851.1:c.655T>A	XP_016856340.1:p.Ser219Thr
XM_017000852.1:c.1498T>A	XP_016856341.1:p.Ser500Thr
NM_201253.3:c.1498T>A MANE Select	NP_957705.1:p.Ser500Thr
NM_001193640.2:c.1162T>A	NP_001180569.1:p.Ser388Thr
NM_001257965.2:c.1291T>A	NP_001244894.1:p.Ser431Thr
NR_047563.2:n.1659T>A
NR_047564.2:n.1659T>A
NM_001257966.2:c.1498T>A	NP_001244895.1:p.Ser500Thr