Canonical Allele Identifier: CA422672597

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403990T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434860T>G , CM000663.2:g.197434860T>G	GRCh38
NC_000001.10:g.197403990T>G , CM000663.1:g.197403990T>G	GRCh37
NC_000001.9:g.195670613T>G	NCBI36
NG_008483.1:g.171583T>G
NG_008483.2:g.238399T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2997T>G MANE Select	ENSP00000356370.3:p.Leu999=
ENST00000638467.1:c.2997T>G	ENSP00000491102.1:p.Leu999=
ENST00000681519.1:c.1878T>G	ENSP00000505267.1:p.Leu626=
ENST00000367397.1:c.1140T>G	ENSP00000356367.1:p.Leu380=
ENST00000367399.6:c.2661T>G	ENSP00000356369.2:p.Leu887=
ENST00000367400.7:c.2997T>G	ENSP00000356370.3:p.Leu999=
ENST00000484075.5:c.2997T>G	ENSP00000433932.1:p.Leu999=
ENST00000535699.5:c.2925T>G	ENSP00000438786.1:p.Leu975=
ENST00000538660.5:c.2129-740T>G	ENSP00000438091.1:n.2129-740T>G
NM_001193640.1:c.2661T>G	NP_001180569.1:p.Leu887=
NM_001257965.1:c.2925T>G	NP_001244894.1:p.Leu975=
NM_001257966.1:c.2129-740T>G	NP_001244895.1:n.2129-740T>G
NM_201253.2:c.2997T>G	NP_957705.1:p.Leu999=
NR_047563.1:n.2998T>G
NR_047564.1:n.3206T>G
XM_011509365.1:c.2997T>G	XP_011507667.1:p.Leu999=
XM_011509366.1:c.2997T>G	XP_011507668.1:p.Leu999=
XM_011509367.1:c.2997T>G	XP_011507669.1:p.Leu999=
XM_011509368.1:c.2415T>G	XP_011507670.1:p.Leu805=
XM_011509369.1:c.1440T>G	XP_011507671.1:p.Leu480=
XM_011509365.2:c.2997T>G	XP_011507667.1:p.Leu999=
XM_011509369.2:c.1440T>G	XP_011507671.1:p.Leu480=
XM_017000851.1:c.2154T>G	XP_016856340.1:p.Leu718=
XM_017000852.1:c.3132T>G	XP_016856341.1:p.Leu1044=
NM_201253.3:c.2997T>G MANE Select	NP_957705.1:p.Leu999=
NM_001193640.2:c.2661T>G	NP_001180569.1:p.Leu887=
NM_001257965.2:c.2925T>G	NP_001244894.1:p.Leu975=
NR_047563.2:n.2950T>G
NR_047564.2:n.3158T>G
NM_001257966.2:c.2129-740T>G	NP_001244895.1:n.2129-740T>G