Canonical Allele Identifier: CA1877946240

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376776_123376778delinsTGA , CM000671.2:g.123376776_123376778delinsTGA	GRCh38
NC_000009.11:g.126139055_126139057delinsTGA , CM000671.1:g.126139055_126139057delinsTGA	GRCh37
NC_000009.10:g.125178876_125178878delinsTGA	NCBI36
NG_051311.1:g.27712_27714delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3634-62_3634-60delinsTGA MANE Select	ENSP00000362734.3:n.3634-62_3634-60delinsTGA
ENST00000373631.7:c.3634-62_3634-60delinsTGA	ENSP00000362734.3:n.3634-62_3634-60delinsTGA
ENST00000460253.1:c.2638-62_2638-60delinsTGA	ENSP00000435279.1:n.2638-62_2638-60delinsTGA
NM_173689.6:c.3634-62_3634-60delinsTGA	NP_775960.4:n.3634-62_3634-60delinsTGA
NR_104603.1:n.2748-62_2748-60delinsTGA
XM_005251934.1:c.2638-62_2638-60delinsTGA	XP_005251991.1:n.2638-62_2638-60delinsTGA
XM_011518556.1:c.3607-62_3607-60delinsTGA	XP_011516858.1:n.3607-62_3607-60delinsTGA
XM_011518557.1:c.3439-62_3439-60delinsTGA	XP_011516859.1:n.3439-62_3439-60delinsTGA
XM_011518558.1:c.3439-62_3439-60delinsTGA	XP_011516860.1:n.3439-62_3439-60delinsTGA
XM_005251934.3:c.2638-62_2638-60delinsTGA	XP_005251991.1:n.2638-62_2638-60delinsTGA
XM_011518556.3:c.3607-62_3607-60delinsTGA	XP_011516858.1:n.3607-62_3607-60delinsTGA
XM_011518557.3:c.3439-62_3439-60delinsTGA	XP_011516859.1:n.3439-62_3439-60delinsTGA
XM_011518558.3:c.3439-62_3439-60delinsTGA	XP_011516860.1:n.3439-62_3439-60delinsTGA
NM_173689.7:c.3634-62_3634-60delinsTGA MANE Select	NP_775960.4:n.3634-62_3634-60delinsTGA
NR_104603.2:n.2748-62_2748-60delinsTGA