Canonical Allele Identifier: CA344040443

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429473G>T , CM000663.2:g.197429473G>T	GRCh38
NC_000001.10:g.197398603G>T , CM000663.1:g.197398603G>T	GRCh37
NC_000001.9:g.195665226G>T	NCBI36
NG_008483.1:g.166196G>T
NG_008483.2:g.233012G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.2701G>T MANE Select	NP_957705.1:p.Val901Phe
ENST00000367400.8:c.2701G>T MANE Select	ENSP00000356370.3:p.Val901Phe
NM_001193640.1:c.2365G>T	NP_001180569.1:p.Val789Phe
NM_001193640.2:c.2365G>T	NP_001180569.1:p.Val789Phe
NM_001257965.1:c.2629G>T	NP_001244894.1:p.Val877Phe
NM_001257965.2:c.2629G>T	NP_001244894.1:p.Val877Phe
NM_001257966.1:c.2129-6127G>T	NP_001244895.1:n.2129-6127G>T
NM_001257966.2:c.2129-6127G>T	NP_001244895.1:n.2129-6127G>T
NM_201253.2:c.2701G>T	NP_957705.1:p.Val901Phe
NR_047563.1:n.2702G>T
NR_047563.2:n.2654G>T
NR_047564.1:n.2910G>T
NR_047564.2:n.2862G>T
ENST00000367397.1:c.844G>T	ENSP00000356367.1:p.Val282Phe
ENST00000367399.6:c.2365G>T	ENSP00000356369.2:p.Val789Phe
ENST00000367400.7:c.2701G>T	ENSP00000356370.3:p.Val901Phe
ENST00000484075.5:c.2701G>T	ENSP00000433932.1:p.Val901Phe
ENST00000535699.5:c.2629G>T	ENSP00000438786.1:p.Val877Phe
ENST00000538660.5:c.2129-6127G>T	ENSP00000438091.1:n.2129-6127G>T
ENST00000638467.1:c.2701G>T	ENSP00000491102.1:p.Val901Phe
ENST00000681519.1:c.1582G>T	ENSP00000505267.1:p.Val528Phe
XM_011509365.1:c.2701G>T	XP_011507667.1:p.Val901Phe
XM_011509365.2:c.2701G>T	XP_011507667.1:p.Val901Phe
XM_011509366.1:c.2701G>T	XP_011507668.1:p.Val901Phe
XM_011509367.1:c.2701G>T	XP_011507669.1:p.Val901Phe
XM_011509368.1:c.2119G>T	XP_011507670.1:p.Val707Phe
XM_011509369.1:c.1144G>T	XP_011507671.1:p.Val382Phe
XM_011509369.2:c.1144G>T	XP_011507671.1:p.Val382Phe
XM_017000851.1:c.1858G>T	XP_016856340.1:p.Val620Phe
XM_017000852.1:c.2836G>T	XP_016856341.1:p.Val946Phe