Canonical Allele Identifier: CA2579446752

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377007_123377009dup , CM000671.2:g.123377007_123377009dup	GRCh38
NC_000009.11:g.126139286_126139288dup , CM000671.1:g.126139286_126139288dup	GRCh37
NC_000009.10:g.125179107_125179109dup	NCBI36
NG_051311.1:g.27943_27945dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3803_3805dup MANE Select	ENSP00000362734.3:p.Ala1268_Arg1269insPro
ENST00000373631.7:c.3803_3805dup	ENSP00000362734.3:p.Ala1268_Arg1269insPro
ENST00000460253.1:c.2807_2809dup	ENSP00000435279.1:p.Ala936_Arg937insPro
NM_173689.6:c.3803_3805dup	NP_775960.4:p.Ala1268_Arg1269insPro
NR_104603.1:n.2917_2919dup
XM_005251934.1:c.2807_2809dup	XP_005251991.1:p.Ala936_Arg937insPro
XM_011518556.1:c.3776_3778dup	XP_011516858.1:p.Ala1259_Arg1260insPro
XM_011518557.1:c.3608_3610dup	XP_011516859.1:p.Ala1203_Arg1204insPro
XM_011518558.1:c.3608_3610dup	XP_011516860.1:p.Ala1203_Arg1204insPro
XM_005251934.3:c.2807_2809dup	XP_005251991.1:p.Ala936_Arg937insPro
XM_011518556.3:c.3776_3778dup	XP_011516858.1:p.Ala1259_Arg1260insPro
XM_011518557.3:c.3608_3610dup	XP_011516859.1:p.Ala1203_Arg1204insPro
XM_011518558.3:c.3608_3610dup	XP_011516860.1:p.Ala1203_Arg1204insPro
NM_173689.7:c.3803_3805dup MANE Select	NP_775960.4:p.Ala1268_Arg1269insPro
NR_104603.2:n.2917_2919dup