Canonical Allele Identifier: CA344035516

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446852T>C (hg19) ; chr1:g.197477722T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477722T>C , CM000663.2:g.197477722T>C	GRCh38
NC_000001.10:g.197446852T>C , CM000663.1:g.197446852T>C	GRCh37
NC_000001.9:g.195713475T>C	NCBI36
NG_008483.1:g.214445T>C
NG_008483.2:g.281261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4064T>C MANE Select	ENSP00000356370.3:p.Leu1355Ser
ENST00000367399.6:c.3728T>C	ENSP00000356369.2:p.Leu1243Ser
ENST00000367400.7:c.4064T>C	ENSP00000356370.3:p.Leu1355Ser
ENST00000448952.1:c.298T>C	ENSP00000395407.1:n.298T>C
ENST00000484075.5:c.*175T>C	ENSP00000433932.1:n.*175T>C
ENST00000535699.5:c.3992T>C	ENSP00000438786.1:p.Leu1331Ser
ENST00000538660.5:c.2456T>C	ENSP00000438091.1:p.Leu819Ser
NM_001193640.1:c.3728T>C	NP_001180569.1:p.Leu1243Ser
NM_001257965.1:c.3992T>C	NP_001244894.1:p.Leu1331Ser
NM_001257966.1:c.2456T>C	NP_001244895.1:p.Leu819Ser
NM_201253.2:c.4064T>C	NP_957705.1:p.Leu1355Ser
NR_047563.1:n.4065T>C
NR_047564.1:n.4515T>C
XM_011509366.1:c.*169T>C	XP_011507668.1:n.*169T>C
XM_011509367.1:c.*43T>C	XP_011507669.1:n.*43T>C
XM_011509368.1:c.3482T>C	XP_011507670.1:p.Leu1161Ser
XM_011509369.1:c.2507T>C	XP_011507671.1:p.Leu836Ser
XM_011509369.2:c.2507T>C	XP_011507671.1:p.Leu836Ser
XM_017000851.1:c.3221T>C	XP_016856340.1:p.Leu1074Ser
XM_017000852.1:c.4199T>C	XP_016856341.1:p.Leu1400Ser
NM_201253.3:c.4064T>C MANE Select	NP_957705.1:p.Leu1355Ser
NM_001193640.2:c.3728T>C	NP_001180569.1:p.Leu1243Ser
NM_001257965.2:c.3992T>C	NP_001244894.1:p.Leu1331Ser
NR_047563.2:n.4017T>C
NR_047564.2:n.4467T>C
NM_001257966.2:c.2456T>C	NP_001244895.1:p.Leu819Ser