Canonical Allele Identifier: CA344047058

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435181T>G , CM000663.2:g.197435181T>G	GRCh38
NC_000001.10:g.197404311T>G , CM000663.1:g.197404311T>G	GRCh37
NC_000001.9:g.195670934T>G	NCBI36
NG_008483.1:g.171904T>G
NG_008483.2:g.238720T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.3318T>G MANE Select	NP_957705.1:p.Tyr1106Ter
ENST00000367400.8:c.3318T>G MANE Select	ENSP00000356370.3:p.Tyr1106Ter
NM_001193640.1:c.2982T>G	NP_001180569.1:p.Tyr994Ter
NM_001193640.2:c.2982T>G	NP_001180569.1:p.Tyr994Ter
NM_001257965.1:c.3246T>G	NP_001244894.1:p.Tyr1082Ter
NM_001257965.2:c.3246T>G	NP_001244894.1:p.Tyr1082Ter
NM_001257966.1:c.2129-419T>G	NP_001244895.1:n.2129-419T>G
NM_001257966.2:c.2129-419T>G	NP_001244895.1:n.2129-419T>G
NM_201253.2:c.3318T>G	NP_957705.1:p.Tyr1106Ter
NR_047563.1:n.3319T>G
NR_047563.2:n.3271T>G
NR_047564.1:n.3527T>G
NR_047564.2:n.3479T>G
ENST00000367397.1:c.1461T>G	ENSP00000356367.1:p.Tyr487Ter
ENST00000367399.6:c.2982T>G	ENSP00000356369.2:p.Tyr994Ter
ENST00000367400.7:c.3318T>G	ENSP00000356370.3:p.Tyr1106Ter
ENST00000484075.5:c.3318T>G	ENSP00000433932.1:p.Tyr1106Ter
ENST00000535699.5:c.3246T>G	ENSP00000438786.1:p.Tyr1082Ter
ENST00000538660.5:c.2129-419T>G	ENSP00000438091.1:n.2129-419T>G
ENST00000638467.1:c.3318T>G	ENSP00000491102.1:p.Tyr1106Ter
ENST00000681519.1:c.2199T>G	ENSP00000505267.1:p.Tyr733Ter
XM_011509365.1:c.3318T>G	XP_011507667.1:p.Tyr1106Ter
XM_011509365.2:c.3318T>G	XP_011507667.1:p.Tyr1106Ter
XM_011509366.1:c.3318T>G	XP_011507668.1:p.Tyr1106Ter
XM_011509367.1:c.3318T>G	XP_011507669.1:p.Tyr1106Ter
XM_011509368.1:c.2736T>G	XP_011507670.1:p.Tyr912Ter
XM_011509369.1:c.1761T>G	XP_011507671.1:p.Tyr587Ter
XM_011509369.2:c.1761T>G	XP_011507671.1:p.Tyr587Ter
XM_017000851.1:c.2475T>G	XP_016856340.1:p.Tyr825Ter
XM_017000852.1:c.3453T>G	XP_016856341.1:p.Tyr1151Ter