Canonical Allele Identifier: CA344045704

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404108C>T (hg19) ; chr1:g.197434978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434978C>T , CM000663.2:g.197434978C>T	GRCh38
NC_000001.10:g.197404108C>T , CM000663.1:g.197404108C>T	GRCh37
NC_000001.9:g.195670731C>T	NCBI36
NG_008483.1:g.171701C>T
NG_008483.2:g.238517C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3115C>T MANE Select	ENSP00000356370.3:p.Leu1039Phe
ENST00000638467.1:c.3115C>T	ENSP00000491102.1:p.Leu1039Phe
ENST00000681519.1:c.1996C>T	ENSP00000505267.1:p.Leu666Phe
ENST00000367397.1:c.1258C>T	ENSP00000356367.1:p.Leu420Phe
ENST00000367399.6:c.2779C>T	ENSP00000356369.2:p.Leu927Phe
ENST00000367400.7:c.3115C>T	ENSP00000356370.3:p.Leu1039Phe
ENST00000484075.5:c.3115C>T	ENSP00000433932.1:p.Leu1039Phe
ENST00000535699.5:c.3043C>T	ENSP00000438786.1:p.Leu1015Phe
ENST00000538660.5:c.2129-622C>T	ENSP00000438091.1:n.2129-622C>T
NM_001193640.1:c.2779C>T	NP_001180569.1:p.Leu927Phe
NM_001257965.1:c.3043C>T	NP_001244894.1:p.Leu1015Phe
NM_001257966.1:c.2129-622C>T	NP_001244895.1:n.2129-622C>T
NM_201253.2:c.3115C>T	NP_957705.1:p.Leu1039Phe
NR_047563.1:n.3116C>T
NR_047564.1:n.3324C>T
XM_011509365.1:c.3115C>T	XP_011507667.1:p.Leu1039Phe
XM_011509366.1:c.3115C>T	XP_011507668.1:p.Leu1039Phe
XM_011509367.1:c.3115C>T	XP_011507669.1:p.Leu1039Phe
XM_011509368.1:c.2533C>T	XP_011507670.1:p.Leu845Phe
XM_011509369.1:c.1558C>T	XP_011507671.1:p.Leu520Phe
XM_011509365.2:c.3115C>T	XP_011507667.1:p.Leu1039Phe
XM_011509369.2:c.1558C>T	XP_011507671.1:p.Leu520Phe
XM_017000851.1:c.2272C>T	XP_016856340.1:p.Leu758Phe
XM_017000852.1:c.3250C>T	XP_016856341.1:p.Leu1084Phe
NM_201253.3:c.3115C>T MANE Select	NP_957705.1:p.Leu1039Phe
NM_001193640.2:c.2779C>T	NP_001180569.1:p.Leu927Phe
NM_001257965.2:c.3043C>T	NP_001244894.1:p.Leu1015Phe
NR_047563.2:n.3068C>T
NR_047564.2:n.3276C>T
NM_001257966.2:c.2129-622C>T	NP_001244895.1:n.2129-622C>T