Canonical Allele Identifier: CA344035499

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446842A>C (hg19) ; chr1:g.197477712A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477712A>C , CM000663.2:g.197477712A>C	GRCh38
NC_000001.10:g.197446842A>C , CM000663.1:g.197446842A>C	GRCh37
NC_000001.9:g.195713465A>C	NCBI36
NG_008483.1:g.214435A>C
NG_008483.2:g.281251A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4054A>C MANE Select	ENSP00000356370.3:p.Thr1352Pro
ENST00000367399.6:c.3718A>C	ENSP00000356369.2:p.Thr1240Pro
ENST00000367400.7:c.4054A>C	ENSP00000356370.3:p.Thr1352Pro
ENST00000448952.1:c.288A>C	ENSP00000395407.1:n.288A>C
ENST00000484075.5:c.*165A>C	ENSP00000433932.1:n.*165A>C
ENST00000535699.5:c.3982A>C	ENSP00000438786.1:p.Thr1328Pro
ENST00000538660.5:c.2446A>C	ENSP00000438091.1:p.Thr816Pro
NM_001193640.1:c.3718A>C	NP_001180569.1:p.Thr1240Pro
NM_001257965.1:c.3982A>C	NP_001244894.1:p.Thr1328Pro
NM_001257966.1:c.2446A>C	NP_001244895.1:p.Thr816Pro
NM_201253.2:c.4054A>C	NP_957705.1:p.Thr1352Pro
NR_047563.1:n.4055A>C
NR_047564.1:n.4505A>C
XM_011509366.1:c.*159A>C	XP_011507668.1:n.*159A>C
XM_011509367.1:c.*33A>C	XP_011507669.1:n.*33A>C
XM_011509368.1:c.3472A>C	XP_011507670.1:p.Thr1158Pro
XM_011509369.1:c.2497A>C	XP_011507671.1:p.Thr833Pro
XM_011509369.2:c.2497A>C	XP_011507671.1:p.Thr833Pro
XM_017000851.1:c.3211A>C	XP_016856340.1:p.Thr1071Pro
XM_017000852.1:c.4189A>C	XP_016856341.1:p.Thr1397Pro
NM_201253.3:c.4054A>C MANE Select	NP_957705.1:p.Thr1352Pro
NM_001193640.2:c.3718A>C	NP_001180569.1:p.Thr1240Pro
NM_001257965.2:c.3982A>C	NP_001244894.1:p.Thr1328Pro
NR_047563.2:n.4007A>C
NR_047564.2:n.4457A>C
NM_001257966.2:c.2446A>C	NP_001244895.1:p.Thr816Pro