Canonical Allele Identifier: CA1311904

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421133A>T , CM000663.2:g.197421133A>T	GRCh38
NC_000001.10:g.197390263A>T , CM000663.1:g.197390263A>T	GRCh37
NC_000001.9:g.195656886A>T	NCBI36
NG_008483.1:g.157856A>T
NG_008483.2:g.224672A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.1305A>T MANE Select	NP_957705.1:p.Gly435=
ENST00000367400.8:c.1305A>T MANE Select	ENSP00000356370.3:p.Gly435=
NM_001193640.1:c.969A>T	NP_001180569.1:p.Gly323=
NM_001193640.2:c.969A>T	NP_001180569.1:p.Gly323=
NM_001257965.1:c.1098A>T	NP_001244894.1:p.Gly366=
NM_001257965.2:c.1098A>T	NP_001244894.1:p.Gly366=
NM_001257966.1:c.1305A>T	NP_001244895.1:p.Gly435=
NM_001257966.2:c.1305A>T	NP_001244895.1:p.Gly435=
NM_201253.2:c.1305A>T	NP_957705.1:p.Gly435=
NR_047563.1:n.1514A>T
NR_047563.2:n.1466A>T
NR_047564.1:n.1514A>T
NR_047564.2:n.1466A>T
ENST00000367397.1:c.-553A>T	ENSP00000356367.1:n.-553A>T
ENST00000367399.6:c.969A>T	ENSP00000356369.2:p.Gly323=
ENST00000367400.7:c.1305A>T	ENSP00000356370.3:p.Gly435=
ENST00000476483.1:n.265A>T
ENST00000484075.5:c.1305A>T	ENSP00000433932.1:p.Gly435=
ENST00000535699.5:c.1098A>T	ENSP00000438786.1:p.Gly366=
ENST00000538660.5:c.1305A>T	ENSP00000438091.1:p.Gly435=
ENST00000638467.1:c.1305A>T	ENSP00000491102.1:p.Gly435=
ENST00000681519.1:c.186A>T	ENSP00000505267.1:p.Gly62=
XM_011509365.1:c.1305A>T	XP_011507667.1:p.Gly435=
XM_011509365.2:c.1305A>T	XP_011507667.1:p.Gly435=
XM_011509366.1:c.1305A>T	XP_011507668.1:p.Gly435=
XM_011509367.1:c.1305A>T	XP_011507669.1:p.Gly435=
XM_011509368.1:c.723A>T	XP_011507670.1:p.Gly241=
XM_011509369.1:c.-253A>T	XP_011507671.1:n.-253A>T
XM_011509369.2:c.-253A>T	XP_011507671.1:n.-253A>T
XM_017000851.1:c.462A>T	XP_016856340.1:p.Gly154=
XM_017000852.1:c.1305A>T	XP_016856341.1:p.Gly435=