Canonical Allele Identifier: CA1877946763

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377027_123377030delinsGTCC , CM000671.2:g.123377027_123377030delinsGTCC	GRCh38
NC_000009.11:g.126139306_126139309delinsGTCC , CM000671.1:g.126139306_126139309delinsGTCC	GRCh37
NC_000009.10:g.125179127_125179130delinsGTCC	NCBI36
NG_051311.1:g.27963_27966delinsGTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3823_3826delinsGTCC MANE Select	ENSP00000362734.3:p.Val1275=
ENST00000373631.7:c.3823_3826delinsGTCC	ENSP00000362734.3:p.Val1275=
ENST00000460253.1:c.2827_2830delinsGTCC	ENSP00000435279.1:p.Val943=
NM_173689.6:c.3823_3826delinsGTCC	NP_775960.4:p.Val1275=
NR_104603.1:n.2937_2940delinsGTCC
XM_005251934.1:c.2827_2830delinsGTCC	XP_005251991.1:p.Val943=
XM_011518556.1:c.3796_3799delinsGTCC	XP_011516858.1:p.Val1266=
XM_011518557.1:c.3628_3631delinsGTCC	XP_011516859.1:p.Val1210=
XM_011518558.1:c.3628_3631delinsGTCC	XP_011516860.1:p.Val1210=
XM_005251934.3:c.2827_2830delinsGTCC	XP_005251991.1:p.Val943=
XM_011518556.3:c.3796_3799delinsGTCC	XP_011516858.1:p.Val1266=
XM_011518557.3:c.3628_3631delinsGTCC	XP_011516859.1:p.Val1210=
XM_011518558.3:c.3628_3631delinsGTCC	XP_011516860.1:p.Val1210=
NM_173689.7:c.3823_3826delinsGTCC MANE Select	NP_775960.4:p.Val1275=
NR_104603.2:n.2937_2940delinsGTCC