Canonical Allele Identifier: CA1877946796

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377043_123377046delinsCGGA , CM000671.2:g.123377043_123377046delinsCGGA	GRCh38
NC_000009.11:g.126139322_126139325delinsCGGA , CM000671.1:g.126139322_126139325delinsCGGA	GRCh37
NC_000009.10:g.125179143_125179146delinsCGGA	NCBI36
NG_051311.1:g.27979_27982delinsCGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3839_3842delinsCGGA MANE Select	ENSP00000362734.3:p.Pro1280=
ENST00000373631.7:c.3839_3842delinsCGGA	ENSP00000362734.3:p.Pro1280=
ENST00000460253.1:c.2843_2846delinsCGGA	ENSP00000435279.1:p.Pro948=
NM_173689.6:c.3839_3842delinsCGGA	NP_775960.4:p.Pro1280=
NR_104603.1:n.2953_2956delinsCGGA
XM_005251934.1:c.2843_2846delinsCGGA	XP_005251991.1:p.Pro948=
XM_011518556.1:c.3812_3815delinsCGGA	XP_011516858.1:p.Pro1271=
XM_011518557.1:c.3644_3647delinsCGGA	XP_011516859.1:p.Pro1215=
XM_011518558.1:c.3644_3647delinsCGGA	XP_011516860.1:p.Pro1215=
XM_005251934.3:c.2843_2846delinsCGGA	XP_005251991.1:p.Pro948=
XM_011518556.3:c.3812_3815delinsCGGA	XP_011516858.1:p.Pro1271=
XM_011518557.3:c.3644_3647delinsCGGA	XP_011516859.1:p.Pro1215=
XM_011518558.3:c.3644_3647delinsCGGA	XP_011516860.1:p.Pro1215=
NM_173689.7:c.3839_3842delinsCGGA MANE Select	NP_775960.4:p.Pro1280=
NR_104603.2:n.2953_2956delinsCGGA