Canonical Allele Identifier: CA344037603

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396926T>C (hg19) ; chr1:g.197427796T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427796T>C , CM000663.2:g.197427796T>C	GRCh38
NC_000001.10:g.197396926T>C , CM000663.1:g.197396926T>C	GRCh37
NC_000001.9:g.195663549T>C	NCBI36
NG_008483.1:g.164519T>C
NG_008483.2:g.231335T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2471T>C MANE Select	ENSP00000356370.3:p.Ile824Thr
ENST00000638467.1:c.2471T>C	ENSP00000491102.1:p.Ile824Thr
ENST00000681519.1:c.1352T>C	ENSP00000505267.1:p.Ile451Thr
ENST00000367397.1:c.614T>C	ENSP00000356367.1:p.Ile205Thr
ENST00000367399.6:c.2135T>C	ENSP00000356369.2:p.Ile712Thr
ENST00000367400.7:c.2471T>C	ENSP00000356370.3:p.Ile824Thr
ENST00000480086.2:n.372T>C
ENST00000484075.5:c.2471T>C	ENSP00000433932.1:p.Ile824Thr
ENST00000535699.5:c.2264T>C	ENSP00000438786.1:p.Ile755Thr
ENST00000538660.5:c.2128+5840T>C	ENSP00000438091.1:n.2128+5840T>C
NM_001193640.1:c.2135T>C	NP_001180569.1:p.Ile712Thr
NM_001257965.1:c.2264T>C	NP_001244894.1:p.Ile755Thr
NM_001257966.1:c.2128+5840T>C	NP_001244895.1:n.2128+5840T>C
NM_201253.2:c.2471T>C	NP_957705.1:p.Ile824Thr
NR_047563.1:n.2472T>C
NR_047564.1:n.2680T>C
XM_011509365.1:c.2471T>C	XP_011507667.1:p.Ile824Thr
XM_011509366.1:c.2471T>C	XP_011507668.1:p.Ile824Thr
XM_011509367.1:c.2471T>C	XP_011507669.1:p.Ile824Thr
XM_011509368.1:c.1889T>C	XP_011507670.1:p.Ile630Thr
XM_011509369.1:c.914T>C	XP_011507671.1:p.Ile305Thr
XM_011509365.2:c.2471T>C	XP_011507667.1:p.Ile824Thr
XM_011509369.2:c.914T>C	XP_011507671.1:p.Ile305Thr
XM_017000851.1:c.1628T>C	XP_016856340.1:p.Ile543Thr
XM_017000852.1:c.2471T>C	XP_016856341.1:p.Ile824Thr
NM_201253.3:c.2471T>C MANE Select	NP_957705.1:p.Ile824Thr
NM_001193640.2:c.2135T>C	NP_001180569.1:p.Ile712Thr
NM_001257965.2:c.2264T>C	NP_001244894.1:p.Ile755Thr
NR_047563.2:n.2424T>C
NR_047564.2:n.2632T>C
NM_001257966.2:c.2128+5840T>C	NP_001244895.1:n.2128+5840T>C