Canonical Allele Identifier: CA344031262

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390472G>C (hg19) ; chr1:g.197421342G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421342G>C , CM000663.2:g.197421342G>C	GRCh38
NC_000001.10:g.197390472G>C , CM000663.1:g.197390472G>C	GRCh37
NC_000001.9:g.195657095G>C	NCBI36
NG_008483.1:g.158065G>C
NG_008483.2:g.224881G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1514G>C MANE Select	ENSP00000356370.3:p.Gly505Ala
ENST00000638467.1:c.1514G>C	ENSP00000491102.1:p.Gly505Ala
ENST00000681519.1:c.395G>C	ENSP00000505267.1:p.Gly132Ala
ENST00000367397.1:c.-344G>C	ENSP00000356367.1:n.-344G>C
ENST00000367399.6:c.1178G>C	ENSP00000356369.2:p.Gly393Ala
ENST00000367400.7:c.1514G>C	ENSP00000356370.3:p.Gly505Ala
ENST00000476483.1:n.474G>C
ENST00000484075.5:c.1514G>C	ENSP00000433932.1:p.Gly505Ala
ENST00000535699.5:c.1307G>C	ENSP00000438786.1:p.Gly436Ala
ENST00000538660.5:c.1514G>C	ENSP00000438091.1:p.Gly505Ala
NM_001193640.1:c.1178G>C	NP_001180569.1:p.Gly393Ala
NM_001257965.1:c.1307G>C	NP_001244894.1:p.Gly436Ala
NM_001257966.1:c.1514G>C	NP_001244895.1:p.Gly505Ala
NM_201253.2:c.1514G>C	NP_957705.1:p.Gly505Ala
NR_047563.1:n.1723G>C
NR_047564.1:n.1723G>C
XM_011509365.1:c.1514G>C	XP_011507667.1:p.Gly505Ala
XM_011509366.1:c.1514G>C	XP_011507668.1:p.Gly505Ala
XM_011509367.1:c.1514G>C	XP_011507669.1:p.Gly505Ala
XM_011509368.1:c.932G>C	XP_011507670.1:p.Gly311Ala
XM_011509369.1:c.-44G>C	XP_011507671.1:n.-44G>C
XM_011509365.2:c.1514G>C	XP_011507667.1:p.Gly505Ala
XM_011509369.2:c.-44G>C	XP_011507671.1:n.-44G>C
XM_017000851.1:c.671G>C	XP_016856340.1:p.Gly224Ala
XM_017000852.1:c.1514G>C	XP_016856341.1:p.Gly505Ala
NM_201253.3:c.1514G>C MANE Select	NP_957705.1:p.Gly505Ala
NM_001193640.2:c.1178G>C	NP_001180569.1:p.Gly393Ala
NM_001257965.2:c.1307G>C	NP_001244894.1:p.Gly436Ala
NR_047563.2:n.1675G>C
NR_047564.2:n.1675G>C
NM_001257966.2:c.1514G>C	NP_001244895.1:p.Gly505Ala