Canonical Allele Identifier: CA422672585

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403981T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434851T>A , CM000663.2:g.197434851T>A	GRCh38
NC_000001.10:g.197403981T>A , CM000663.1:g.197403981T>A	GRCh37
NC_000001.9:g.195670604T>A	NCBI36
NG_008483.1:g.171574T>A
NG_008483.2:g.238390T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2988T>A MANE Select	ENSP00000356370.3:p.Pro996=
ENST00000638467.1:c.2988T>A	ENSP00000491102.1:p.Pro996=
ENST00000681519.1:c.1869T>A	ENSP00000505267.1:p.Pro623=
ENST00000367397.1:c.1131T>A	ENSP00000356367.1:p.Pro377=
ENST00000367399.6:c.2652T>A	ENSP00000356369.2:p.Pro884=
ENST00000367400.7:c.2988T>A	ENSP00000356370.3:p.Pro996=
ENST00000484075.5:c.2988T>A	ENSP00000433932.1:p.Pro996=
ENST00000535699.5:c.2916T>A	ENSP00000438786.1:p.Pro972=
ENST00000538660.5:c.2129-749T>A	ENSP00000438091.1:n.2129-749T>A
NM_001193640.1:c.2652T>A	NP_001180569.1:p.Pro884=
NM_001257965.1:c.2916T>A	NP_001244894.1:p.Pro972=
NM_001257966.1:c.2129-749T>A	NP_001244895.1:n.2129-749T>A
NM_201253.2:c.2988T>A	NP_957705.1:p.Pro996=
NR_047563.1:n.2989T>A
NR_047564.1:n.3197T>A
XM_011509365.1:c.2988T>A	XP_011507667.1:p.Pro996=
XM_011509366.1:c.2988T>A	XP_011507668.1:p.Pro996=
XM_011509367.1:c.2988T>A	XP_011507669.1:p.Pro996=
XM_011509368.1:c.2406T>A	XP_011507670.1:p.Pro802=
XM_011509369.1:c.1431T>A	XP_011507671.1:p.Pro477=
XM_011509365.2:c.2988T>A	XP_011507667.1:p.Pro996=
XM_011509369.2:c.1431T>A	XP_011507671.1:p.Pro477=
XM_017000851.1:c.2145T>A	XP_016856340.1:p.Pro715=
XM_017000852.1:c.3123T>A	XP_016856341.1:p.Pro1041=
NM_201253.3:c.2988T>A MANE Select	NP_957705.1:p.Pro996=
NM_001193640.2:c.2652T>A	NP_001180569.1:p.Pro884=
NM_001257965.2:c.2916T>A	NP_001244894.1:p.Pro972=
NR_047563.2:n.2941T>A
NR_047564.2:n.3149T>A
NM_001257966.2:c.2129-749T>A	NP_001244895.1:n.2129-749T>A