Canonical Allele Identifier: CA1877946455

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376902_123376906delinsGCCTC , CM000671.2:g.123376902_123376906delinsGCCTC	GRCh38
NC_000009.11:g.126139181_126139185delinsGCCTC , CM000671.1:g.126139181_126139185delinsGCCTC	GRCh37
NC_000009.10:g.125179002_125179006delinsGCCTC	NCBI36
NG_051311.1:g.27838_27842delinsGCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3698_3702delinsGCCTC MANE Select	ENSP00000362734.3:p.Cys1233=
ENST00000373631.7:c.3698_3702delinsGCCTC	ENSP00000362734.3:p.Cys1233=
ENST00000460253.1:c.2702_2706delinsGCCTC	ENSP00000435279.1:p.Cys901=
NM_173689.6:c.3698_3702delinsGCCTC	NP_775960.4:p.Cys1233=
NR_104603.1:n.2812_2816delinsGCCTC
XM_005251934.1:c.2702_2706delinsGCCTC	XP_005251991.1:p.Cys901=
XM_011518556.1:c.3671_3675delinsGCCTC	XP_011516858.1:p.Cys1224=
XM_011518557.1:c.3503_3507delinsGCCTC	XP_011516859.1:p.Cys1168=
XM_011518558.1:c.3503_3507delinsGCCTC	XP_011516860.1:p.Cys1168=
XM_005251934.3:c.2702_2706delinsGCCTC	XP_005251991.1:p.Cys901=
XM_011518556.3:c.3671_3675delinsGCCTC	XP_011516858.1:p.Cys1224=
XM_011518557.3:c.3503_3507delinsGCCTC	XP_011516859.1:p.Cys1168=
XM_011518558.3:c.3503_3507delinsGCCTC	XP_011516860.1:p.Cys1168=
NM_173689.7:c.3698_3702delinsGCCTC MANE Select	NP_775960.4:p.Cys1233=
NR_104603.2:n.2812_2816delinsGCCTC