Canonical Allele Identifier: CA653866676

Gene: CRB2

Linked Data

• COSMIC: COSN20076876

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377074_123377075insA , CM000671.2:g.123377074_123377075insA	GRCh38
NC_000009.11:g.126139353_126139354insA , CM000671.1:g.126139353_126139354insA	GRCh37
NC_000009.10:g.125179174_125179175insA	NCBI36
NG_051311.1:g.28010_28011insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*12_*13insA MANE Select	ENSP00000362734.3:n.*12_*13insA
ENST00000373631.7:c.*12_*13insA	ENSP00000362734.3:n.*12_*13insA
ENST00000460253.1:c.*12_*13insA	ENSP00000435279.1:n.*12_*13insA
NM_173689.6:c.*12_*13insA	NP_775960.4:n.*12_*13insA
NR_104603.1:n.2984_2985insA
XM_005251934.1:c.*12_*13insA	XP_005251991.1:n.*12_*13insA
XM_011518556.1:c.*12_*13insA	XP_011516858.1:n.*12_*13insA
XM_011518557.1:c.*12_*13insA	XP_011516859.1:n.*12_*13insA
XM_011518558.1:c.*12_*13insA	XP_011516860.1:n.*12_*13insA
XM_005251934.3:c.*12_*13insA	XP_005251991.1:n.*12_*13insA
XM_011518556.3:c.*12_*13insA	XP_011516858.1:n.*12_*13insA
XM_011518557.3:c.*12_*13insA	XP_011516859.1:n.*12_*13insA
XM_011518558.3:c.*12_*13insA	XP_011516860.1:n.*12_*13insA
NM_173689.7:c.*12_*13insA MANE Select	NP_775960.4:n.*12_*13insA
NR_104603.2:n.2984_2985insA