Canonical Allele Identifier: CA344037164

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396858G>C (hg19) ; chr1:g.197427728G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427728G>C , CM000663.2:g.197427728G>C	GRCh38
NC_000001.10:g.197396858G>C , CM000663.1:g.197396858G>C	GRCh37
NC_000001.9:g.195663481G>C	NCBI36
NG_008483.1:g.164451G>C
NG_008483.2:g.231267G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.2403G>C MANE Select	ENSP00000356370.3:p.Lys801Asn
ENST00000638467.1:c.2403G>C	ENSP00000491102.1:p.Lys801Asn
ENST00000681519.1:c.1284G>C	ENSP00000505267.1:p.Lys428Asn
ENST00000367397.1:c.546G>C	ENSP00000356367.1:p.Lys182Asn
ENST00000367399.6:c.2067G>C	ENSP00000356369.2:p.Lys689Asn
ENST00000367400.7:c.2403G>C	ENSP00000356370.3:p.Lys801Asn
ENST00000480086.2:n.304G>C
ENST00000484075.5:c.2403G>C	ENSP00000433932.1:p.Lys801Asn
ENST00000535699.5:c.2196G>C	ENSP00000438786.1:p.Lys732Asn
ENST00000538660.5:c.2128+5772G>C	ENSP00000438091.1:n.2128+5772G>C
NM_001193640.1:c.2067G>C	NP_001180569.1:p.Lys689Asn
NM_001257965.1:c.2196G>C	NP_001244894.1:p.Lys732Asn
NM_001257966.1:c.2128+5772G>C	NP_001244895.1:n.2128+5772G>C
NM_201253.2:c.2403G>C	NP_957705.1:p.Lys801Asn
NR_047563.1:n.2404G>C
NR_047564.1:n.2612G>C
XM_011509365.1:c.2403G>C	XP_011507667.1:p.Lys801Asn
XM_011509366.1:c.2403G>C	XP_011507668.1:p.Lys801Asn
XM_011509367.1:c.2403G>C	XP_011507669.1:p.Lys801Asn
XM_011509368.1:c.1821G>C	XP_011507670.1:p.Lys607Asn
XM_011509369.1:c.846G>C	XP_011507671.1:p.Lys282Asn
XM_011509365.2:c.2403G>C	XP_011507667.1:p.Lys801Asn
XM_011509369.2:c.846G>C	XP_011507671.1:p.Lys282Asn
XM_017000851.1:c.1560G>C	XP_016856340.1:p.Lys520Asn
XM_017000852.1:c.2403G>C	XP_016856341.1:p.Lys801Asn
NM_201253.3:c.2403G>C MANE Select	NP_957705.1:p.Lys801Asn
NM_001193640.2:c.2067G>C	NP_001180569.1:p.Lys689Asn
NM_001257965.2:c.2196G>C	NP_001244894.1:p.Lys732Asn
NR_047563.2:n.2356G>C
NR_047564.2:n.2564G>C
NM_001257966.2:c.2128+5772G>C	NP_001244895.1:n.2128+5772G>C