Canonical Allele Identifier: CA344032779

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390820C>G (hg19) ; chr1:g.197421690C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421690C>G , CM000663.2:g.197421690C>G	GRCh38
NC_000001.10:g.197390820C>G , CM000663.1:g.197390820C>G	GRCh37
NC_000001.9:g.195657443C>G	NCBI36
NG_008483.1:g.158413C>G
NG_008483.2:g.225229C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1862C>G MANE Select	ENSP00000356370.3:p.Thr621Ser
ENST00000638467.1:c.1862C>G	ENSP00000491102.1:p.Thr621Ser
ENST00000681519.1:c.743C>G	ENSP00000505267.1:p.Thr248Ser
ENST00000367397.1:c.5C>G	ENSP00000356367.1:p.Thr2Ser
ENST00000367399.6:c.1526C>G	ENSP00000356369.2:p.Thr509Ser
ENST00000367400.7:c.1862C>G	ENSP00000356370.3:p.Thr621Ser
ENST00000484075.5:c.1862C>G	ENSP00000433932.1:p.Thr621Ser
ENST00000535699.5:c.1655C>G	ENSP00000438786.1:p.Thr552Ser
ENST00000538660.5:c.1862C>G	ENSP00000438091.1:p.Thr621Ser
NM_001193640.1:c.1526C>G	NP_001180569.1:p.Thr509Ser
NM_001257965.1:c.1655C>G	NP_001244894.1:p.Thr552Ser
NM_001257966.1:c.1862C>G	NP_001244895.1:p.Thr621Ser
NM_201253.2:c.1862C>G	NP_957705.1:p.Thr621Ser
NR_047563.1:n.1923-60C>G
NR_047564.1:n.2071C>G
XM_011509365.1:c.1862C>G	XP_011507667.1:p.Thr621Ser
XM_011509366.1:c.1862C>G	XP_011507668.1:p.Thr621Ser
XM_011509367.1:c.1862C>G	XP_011507669.1:p.Thr621Ser
XM_011509368.1:c.1280C>G	XP_011507670.1:p.Thr427Ser
XM_011509369.1:c.305C>G	XP_011507671.1:p.Thr102Ser
XM_011509365.2:c.1862C>G	XP_011507667.1:p.Thr621Ser
XM_011509369.2:c.305C>G	XP_011507671.1:p.Thr102Ser
XM_017000851.1:c.1019C>G	XP_016856340.1:p.Thr340Ser
XM_017000852.1:c.1862C>G	XP_016856341.1:p.Thr621Ser
NM_201253.3:c.1862C>G MANE Select	NP_957705.1:p.Thr621Ser
NM_001193640.2:c.1526C>G	NP_001180569.1:p.Thr509Ser
NM_001257965.2:c.1655C>G	NP_001244894.1:p.Thr552Ser
NR_047563.2:n.1875-60C>G
NR_047564.2:n.2023C>G
NM_001257966.2:c.1862C>G	NP_001244895.1:p.Thr621Ser