Canonical Allele Identifier: CA344047601

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404396A>C (hg19) ; chr1:g.197435266A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435266A>C , CM000663.2:g.197435266A>C	GRCh38
NC_000001.10:g.197404396A>C , CM000663.1:g.197404396A>C	GRCh37
NC_000001.9:g.195671019A>C	NCBI36
NG_008483.1:g.171989A>C
NG_008483.2:g.238805A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3403A>C MANE Select	ENSP00000356370.3:p.Thr1135Pro
ENST00000638467.1:c.3403A>C	ENSP00000491102.1:p.Thr1135Pro
ENST00000681519.1:c.2284A>C	ENSP00000505267.1:p.Thr762Pro
ENST00000367397.1:c.1546A>C	ENSP00000356367.1:p.Thr516Pro
ENST00000367399.6:c.3067A>C	ENSP00000356369.2:p.Thr1023Pro
ENST00000367400.7:c.3403A>C	ENSP00000356370.3:p.Thr1135Pro
ENST00000484075.5:c.3403A>C	ENSP00000433932.1:p.Thr1135Pro
ENST00000535699.5:c.3331A>C	ENSP00000438786.1:p.Thr1111Pro
ENST00000538660.5:c.2129-334A>C	ENSP00000438091.1:n.2129-334A>C
NM_001193640.1:c.3067A>C	NP_001180569.1:p.Thr1023Pro
NM_001257965.1:c.3331A>C	NP_001244894.1:p.Thr1111Pro
NM_001257966.1:c.2129-334A>C	NP_001244895.1:n.2129-334A>C
NM_201253.2:c.3403A>C	NP_957705.1:p.Thr1135Pro
NR_047563.1:n.3404A>C
NR_047564.1:n.3612A>C
XM_011509365.1:c.3403A>C	XP_011507667.1:p.Thr1135Pro
XM_011509366.1:c.3403A>C	XP_011507668.1:p.Thr1135Pro
XM_011509367.1:c.3403A>C	XP_011507669.1:p.Thr1135Pro
XM_011509368.1:c.2821A>C	XP_011507670.1:p.Thr941Pro
XM_011509369.1:c.1846A>C	XP_011507671.1:p.Thr616Pro
XM_011509365.2:c.3403A>C	XP_011507667.1:p.Thr1135Pro
XM_011509369.2:c.1846A>C	XP_011507671.1:p.Thr616Pro
XM_017000851.1:c.2560A>C	XP_016856340.1:p.Thr854Pro
XM_017000852.1:c.3538A>C	XP_016856341.1:p.Thr1180Pro
NM_201253.3:c.3403A>C MANE Select	NP_957705.1:p.Thr1135Pro
NM_001193640.2:c.3067A>C	NP_001180569.1:p.Thr1023Pro
NM_001257965.2:c.3331A>C	NP_001244894.1:p.Thr1111Pro
NR_047563.2:n.3356A>C
NR_047564.2:n.3564A>C
NM_001257966.2:c.2129-334A>C	NP_001244895.1:n.2129-334A>C