Canonical Allele Identifier: CA344047237

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404343T>G (hg19) ; chr1:g.197435213T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435213T>G , CM000663.2:g.197435213T>G	GRCh38
NC_000001.10:g.197404343T>G , CM000663.1:g.197404343T>G	GRCh37
NC_000001.9:g.195670966T>G	NCBI36
NG_008483.1:g.171936T>G
NG_008483.2:g.238752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3350T>G MANE Select	ENSP00000356370.3:p.Ile1117Ser
ENST00000638467.1:c.3350T>G	ENSP00000491102.1:p.Ile1117Ser
ENST00000681519.1:c.2231T>G	ENSP00000505267.1:p.Ile744Ser
ENST00000367397.1:c.1493T>G	ENSP00000356367.1:p.Ile498Ser
ENST00000367399.6:c.3014T>G	ENSP00000356369.2:p.Ile1005Ser
ENST00000367400.7:c.3350T>G	ENSP00000356370.3:p.Ile1117Ser
ENST00000484075.5:c.3350T>G	ENSP00000433932.1:p.Ile1117Ser
ENST00000535699.5:c.3278T>G	ENSP00000438786.1:p.Ile1093Ser
ENST00000538660.5:c.2129-387T>G	ENSP00000438091.1:n.2129-387T>G
NM_001193640.1:c.3014T>G	NP_001180569.1:p.Ile1005Ser
NM_001257965.1:c.3278T>G	NP_001244894.1:p.Ile1093Ser
NM_001257966.1:c.2129-387T>G	NP_001244895.1:n.2129-387T>G
NM_201253.2:c.3350T>G	NP_957705.1:p.Ile1117Ser
NR_047563.1:n.3351T>G
NR_047564.1:n.3559T>G
XM_011509365.1:c.3350T>G	XP_011507667.1:p.Ile1117Ser
XM_011509366.1:c.3350T>G	XP_011507668.1:p.Ile1117Ser
XM_011509367.1:c.3350T>G	XP_011507669.1:p.Ile1117Ser
XM_011509368.1:c.2768T>G	XP_011507670.1:p.Ile923Ser
XM_011509369.1:c.1793T>G	XP_011507671.1:p.Ile598Ser
XM_011509365.2:c.3350T>G	XP_011507667.1:p.Ile1117Ser
XM_011509369.2:c.1793T>G	XP_011507671.1:p.Ile598Ser
XM_017000851.1:c.2507T>G	XP_016856340.1:p.Ile836Ser
XM_017000852.1:c.3485T>G	XP_016856341.1:p.Ile1162Ser
NM_201253.3:c.3350T>G MANE Select	NP_957705.1:p.Ile1117Ser
NM_001193640.2:c.3014T>G	NP_001180569.1:p.Ile1005Ser
NM_001257965.2:c.3278T>G	NP_001244894.1:p.Ile1093Ser
NR_047563.2:n.3303T>G
NR_047564.2:n.3511T>G
NM_001257966.2:c.2129-387T>G	NP_001244895.1:n.2129-387T>G