Canonical Allele Identifier: CA344031426

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390508T>A (hg19) ; chr1:g.197421378T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421378T>A , CM000663.2:g.197421378T>A	GRCh38
NC_000001.10:g.197390508T>A , CM000663.1:g.197390508T>A	GRCh37
NC_000001.9:g.195657131T>A	NCBI36
NG_008483.1:g.158101T>A
NG_008483.2:g.224917T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1550T>A MANE Select	ENSP00000356370.3:p.Val517Asp
ENST00000638467.1:c.1550T>A	ENSP00000491102.1:p.Val517Asp
ENST00000681519.1:c.431T>A	ENSP00000505267.1:p.Val144Asp
ENST00000367397.1:c.-308T>A	ENSP00000356367.1:n.-308T>A
ENST00000367399.6:c.1214T>A	ENSP00000356369.2:p.Val405Asp
ENST00000367400.7:c.1550T>A	ENSP00000356370.3:p.Val517Asp
ENST00000476483.1:n.510T>A
ENST00000484075.5:c.1550T>A	ENSP00000433932.1:p.Val517Asp
ENST00000535699.5:c.1343T>A	ENSP00000438786.1:p.Val448Asp
ENST00000538660.5:c.1550T>A	ENSP00000438091.1:p.Val517Asp
NM_001193640.1:c.1214T>A	NP_001180569.1:p.Val405Asp
NM_001257965.1:c.1343T>A	NP_001244894.1:p.Val448Asp
NM_001257966.1:c.1550T>A	NP_001244895.1:p.Val517Asp
NM_201253.2:c.1550T>A	NP_957705.1:p.Val517Asp
NR_047563.1:n.1759T>A
NR_047564.1:n.1759T>A
XM_011509365.1:c.1550T>A	XP_011507667.1:p.Val517Asp
XM_011509366.1:c.1550T>A	XP_011507668.1:p.Val517Asp
XM_011509367.1:c.1550T>A	XP_011507669.1:p.Val517Asp
XM_011509368.1:c.968T>A	XP_011507670.1:p.Val323Asp
XM_011509369.1:c.-8T>A	XP_011507671.1:n.-8T>A
XM_011509365.2:c.1550T>A	XP_011507667.1:p.Val517Asp
XM_011509369.2:c.-8T>A	XP_011507671.1:n.-8T>A
XM_017000851.1:c.707T>A	XP_016856340.1:p.Val236Asp
XM_017000852.1:c.1550T>A	XP_016856341.1:p.Val517Asp
NM_201253.3:c.1550T>A MANE Select	NP_957705.1:p.Val517Asp
NM_001193640.2:c.1214T>A	NP_001180569.1:p.Val405Asp
NM_001257965.2:c.1343T>A	NP_001244894.1:p.Val448Asp
NR_047563.2:n.1711T>A
NR_047564.2:n.1711T>A
NM_001257966.2:c.1550T>A	NP_001244895.1:p.Val517Asp