Canonical Allele Identifier: CA344045343

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404079T>G (hg19) ; chr1:g.197434949T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434949T>G , CM000663.2:g.197434949T>G	GRCh38
NC_000001.10:g.197404079T>G , CM000663.1:g.197404079T>G	GRCh37
NC_000001.9:g.195670702T>G	NCBI36
NG_008483.1:g.171672T>G
NG_008483.2:g.238488T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3086T>G MANE Select	ENSP00000356370.3:p.Val1029Gly
ENST00000638467.1:c.3086T>G	ENSP00000491102.1:p.Val1029Gly
ENST00000681519.1:c.1967T>G	ENSP00000505267.1:p.Val656Gly
ENST00000367397.1:c.1229T>G	ENSP00000356367.1:p.Val410Gly
ENST00000367399.6:c.2750T>G	ENSP00000356369.2:p.Val917Gly
ENST00000367400.7:c.3086T>G	ENSP00000356370.3:p.Val1029Gly
ENST00000484075.5:c.3086T>G	ENSP00000433932.1:p.Val1029Gly
ENST00000535699.5:c.3014T>G	ENSP00000438786.1:p.Val1005Gly
ENST00000538660.5:c.2129-651T>G	ENSP00000438091.1:n.2129-651T>G
NM_001193640.1:c.2750T>G	NP_001180569.1:p.Val917Gly
NM_001257965.1:c.3014T>G	NP_001244894.1:p.Val1005Gly
NM_001257966.1:c.2129-651T>G	NP_001244895.1:n.2129-651T>G
NM_201253.2:c.3086T>G	NP_957705.1:p.Val1029Gly
NR_047563.1:n.3087T>G
NR_047564.1:n.3295T>G
XM_011509365.1:c.3086T>G	XP_011507667.1:p.Val1029Gly
XM_011509366.1:c.3086T>G	XP_011507668.1:p.Val1029Gly
XM_011509367.1:c.3086T>G	XP_011507669.1:p.Val1029Gly
XM_011509368.1:c.2504T>G	XP_011507670.1:p.Val835Gly
XM_011509369.1:c.1529T>G	XP_011507671.1:p.Val510Gly
XM_011509365.2:c.3086T>G	XP_011507667.1:p.Val1029Gly
XM_011509369.2:c.1529T>G	XP_011507671.1:p.Val510Gly
XM_017000851.1:c.2243T>G	XP_016856340.1:p.Val748Gly
XM_017000852.1:c.3221T>G	XP_016856341.1:p.Val1074Gly
NM_201253.3:c.3086T>G MANE Select	NP_957705.1:p.Val1029Gly
NM_001193640.2:c.2750T>G	NP_001180569.1:p.Val917Gly
NM_001257965.2:c.3014T>G	NP_001244894.1:p.Val1005Gly
NR_047563.2:n.3039T>G
NR_047564.2:n.3247T>G
NM_001257966.2:c.2129-651T>G	NP_001244895.1:n.2129-651T>G