Canonical Allele Identifier: CA344044789

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404028T>G (hg19) ; chr1:g.197434898T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434898T>G , CM000663.2:g.197434898T>G	GRCh38
NC_000001.10:g.197404028T>G , CM000663.1:g.197404028T>G	GRCh37
NC_000001.9:g.195670651T>G	NCBI36
NG_008483.1:g.171621T>G
NG_008483.2:g.238437T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3035T>G MANE Select	ENSP00000356370.3:p.Leu1012Trp
ENST00000638467.1:c.3035T>G	ENSP00000491102.1:p.Leu1012Trp
ENST00000681519.1:c.1916T>G	ENSP00000505267.1:p.Leu639Trp
ENST00000367397.1:c.1178T>G	ENSP00000356367.1:p.Leu393Trp
ENST00000367399.6:c.2699T>G	ENSP00000356369.2:p.Leu900Trp
ENST00000367400.7:c.3035T>G	ENSP00000356370.3:p.Leu1012Trp
ENST00000484075.5:c.3035T>G	ENSP00000433932.1:p.Leu1012Trp
ENST00000535699.5:c.2963T>G	ENSP00000438786.1:p.Leu988Trp
ENST00000538660.5:c.2129-702T>G	ENSP00000438091.1:n.2129-702T>G
NM_001193640.1:c.2699T>G	NP_001180569.1:p.Leu900Trp
NM_001257965.1:c.2963T>G	NP_001244894.1:p.Leu988Trp
NM_001257966.1:c.2129-702T>G	NP_001244895.1:n.2129-702T>G
NM_201253.2:c.3035T>G	NP_957705.1:p.Leu1012Trp
NR_047563.1:n.3036T>G
NR_047564.1:n.3244T>G
XM_011509365.1:c.3035T>G	XP_011507667.1:p.Leu1012Trp
XM_011509366.1:c.3035T>G	XP_011507668.1:p.Leu1012Trp
XM_011509367.1:c.3035T>G	XP_011507669.1:p.Leu1012Trp
XM_011509368.1:c.2453T>G	XP_011507670.1:p.Leu818Trp
XM_011509369.1:c.1478T>G	XP_011507671.1:p.Leu493Trp
XM_011509365.2:c.3035T>G	XP_011507667.1:p.Leu1012Trp
XM_011509369.2:c.1478T>G	XP_011507671.1:p.Leu493Trp
XM_017000851.1:c.2192T>G	XP_016856340.1:p.Leu731Trp
XM_017000852.1:c.3170T>G	XP_016856341.1:p.Leu1057Trp
NM_201253.3:c.3035T>G MANE Select	NP_957705.1:p.Leu1012Trp
NM_001193640.2:c.2699T>G	NP_001180569.1:p.Leu900Trp
NM_001257965.2:c.2963T>G	NP_001244894.1:p.Leu988Trp
NR_047563.2:n.2988T>G
NR_047564.2:n.3196T>G
NM_001257966.2:c.2129-702T>G	NP_001244895.1:n.2129-702T>G