Canonical Allele Identifier: CA344036067

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446993T>G (hg19) ; chr1:g.197477863T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477863T>G , CM000663.2:g.197477863T>G	GRCh38
NC_000001.10:g.197446993T>G , CM000663.1:g.197446993T>G	GRCh37
NC_000001.9:g.195713616T>G	NCBI36
NG_008483.1:g.214586T>G
NG_008483.2:g.281402T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4205T>G MANE Select	ENSP00000356370.3:p.Met1402Arg
ENST00000367399.6:c.3869T>G	ENSP00000356369.2:p.Met1290Arg
ENST00000367400.7:c.4205T>G	ENSP00000356370.3:p.Met1402Arg
ENST00000448952.1:c.439T>G	ENSP00000395407.1:n.439T>G
ENST00000484075.5:c.*316T>G	ENSP00000433932.1:n.*316T>G
ENST00000535699.5:c.4133T>G	ENSP00000438786.1:p.Met1378Arg
ENST00000538660.5:c.2597T>G	ENSP00000438091.1:p.Met866Arg
NM_001193640.1:c.3869T>G	NP_001180569.1:p.Met1290Arg
NM_001257965.1:c.4133T>G	NP_001244894.1:p.Met1378Arg
NM_001257966.1:c.2597T>G	NP_001244895.1:p.Met866Arg
NM_201253.2:c.4205T>G	NP_957705.1:p.Met1402Arg
NR_047563.1:n.4206T>G
NR_047564.1:n.4656T>G
XM_011509366.1:c.*310T>G	XP_011507668.1:n.*310T>G
XM_011509367.1:c.*184T>G	XP_011507669.1:n.*184T>G
XM_011509368.1:c.3623T>G	XP_011507670.1:p.Met1208Arg
XM_011509369.1:c.2648T>G	XP_011507671.1:p.Met883Arg
XM_011509369.2:c.2648T>G	XP_011507671.1:p.Met883Arg
XM_017000851.1:c.3362T>G	XP_016856340.1:p.Met1121Arg
XM_017000852.1:c.4340T>G	XP_016856341.1:p.Met1447Arg
NM_201253.3:c.4205T>G MANE Select	NP_957705.1:p.Met1402Arg
NM_001193640.2:c.3869T>G	NP_001180569.1:p.Met1290Arg
NM_001257965.2:c.4133T>G	NP_001244894.1:p.Met1378Arg
NR_047563.2:n.4158T>G
NR_047564.2:n.4608T>G
NM_001257966.2:c.2597T>G	NP_001244895.1:p.Met866Arg