Canonical Allele Identifier: CA344047150

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404328A>G (hg19) ; chr1:g.197435198A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435198A>G , CM000663.2:g.197435198A>G	GRCh38
NC_000001.10:g.197404328A>G , CM000663.1:g.197404328A>G	GRCh37
NC_000001.9:g.195670951A>G	NCBI36
NG_008483.1:g.171921A>G
NG_008483.2:g.238737A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3335A>G MANE Select	ENSP00000356370.3:p.Asn1112Ser
ENST00000638467.1:c.3335A>G	ENSP00000491102.1:p.Asn1112Ser
ENST00000681519.1:c.2216A>G	ENSP00000505267.1:p.Asn739Ser
ENST00000367397.1:c.1478A>G	ENSP00000356367.1:p.Asn493Ser
ENST00000367399.6:c.2999A>G	ENSP00000356369.2:p.Asn1000Ser
ENST00000367400.7:c.3335A>G	ENSP00000356370.3:p.Asn1112Ser
ENST00000484075.5:c.3335A>G	ENSP00000433932.1:p.Asn1112Ser
ENST00000535699.5:c.3263A>G	ENSP00000438786.1:p.Asn1088Ser
ENST00000538660.5:c.2129-402A>G	ENSP00000438091.1:n.2129-402A>G
NM_001193640.1:c.2999A>G	NP_001180569.1:p.Asn1000Ser
NM_001257965.1:c.3263A>G	NP_001244894.1:p.Asn1088Ser
NM_001257966.1:c.2129-402A>G	NP_001244895.1:n.2129-402A>G
NM_201253.2:c.3335A>G	NP_957705.1:p.Asn1112Ser
NR_047563.1:n.3336A>G
NR_047564.1:n.3544A>G
XM_011509365.1:c.3335A>G	XP_011507667.1:p.Asn1112Ser
XM_011509366.1:c.3335A>G	XP_011507668.1:p.Asn1112Ser
XM_011509367.1:c.3335A>G	XP_011507669.1:p.Asn1112Ser
XM_011509368.1:c.2753A>G	XP_011507670.1:p.Asn918Ser
XM_011509369.1:c.1778A>G	XP_011507671.1:p.Asn593Ser
XM_011509365.2:c.3335A>G	XP_011507667.1:p.Asn1112Ser
XM_011509369.2:c.1778A>G	XP_011507671.1:p.Asn593Ser
XM_017000851.1:c.2492A>G	XP_016856340.1:p.Asn831Ser
XM_017000852.1:c.3470A>G	XP_016856341.1:p.Asn1157Ser
NM_201253.3:c.3335A>G MANE Select	NP_957705.1:p.Asn1112Ser
NM_001193640.2:c.2999A>G	NP_001180569.1:p.Asn1000Ser
NM_001257965.2:c.3263A>G	NP_001244894.1:p.Asn1088Ser
NR_047563.2:n.3288A>G
NR_047564.2:n.3496A>G
NM_001257966.2:c.2129-402A>G	NP_001244895.1:n.2129-402A>G