Canonical Allele Identifier: CA344047249

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404346A>T (hg19) ; chr1:g.197435216A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435216A>T , CM000663.2:g.197435216A>T	GRCh38
NC_000001.10:g.197404346A>T , CM000663.1:g.197404346A>T	GRCh37
NC_000001.9:g.195670969A>T	NCBI36
NG_008483.1:g.171939A>T
NG_008483.2:g.238755A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3353A>T MANE Select	ENSP00000356370.3:p.Asn1118Ile
ENST00000638467.1:c.3353A>T	ENSP00000491102.1:p.Asn1118Ile
ENST00000681519.1:c.2234A>T	ENSP00000505267.1:p.Asn745Ile
ENST00000367397.1:c.1496A>T	ENSP00000356367.1:p.Asn499Ile
ENST00000367399.6:c.3017A>T	ENSP00000356369.2:p.Asn1006Ile
ENST00000367400.7:c.3353A>T	ENSP00000356370.3:p.Asn1118Ile
ENST00000484075.5:c.3353A>T	ENSP00000433932.1:p.Asn1118Ile
ENST00000535699.5:c.3281A>T	ENSP00000438786.1:p.Asn1094Ile
ENST00000538660.5:c.2129-384A>T	ENSP00000438091.1:n.2129-384A>T
NM_001193640.1:c.3017A>T	NP_001180569.1:p.Asn1006Ile
NM_001257965.1:c.3281A>T	NP_001244894.1:p.Asn1094Ile
NM_001257966.1:c.2129-384A>T	NP_001244895.1:n.2129-384A>T
NM_201253.2:c.3353A>T	NP_957705.1:p.Asn1118Ile
NR_047563.1:n.3354A>T
NR_047564.1:n.3562A>T
XM_011509365.1:c.3353A>T	XP_011507667.1:p.Asn1118Ile
XM_011509366.1:c.3353A>T	XP_011507668.1:p.Asn1118Ile
XM_011509367.1:c.3353A>T	XP_011507669.1:p.Asn1118Ile
XM_011509368.1:c.2771A>T	XP_011507670.1:p.Asn924Ile
XM_011509369.1:c.1796A>T	XP_011507671.1:p.Asn599Ile
XM_011509365.2:c.3353A>T	XP_011507667.1:p.Asn1118Ile
XM_011509369.2:c.1796A>T	XP_011507671.1:p.Asn599Ile
XM_017000851.1:c.2510A>T	XP_016856340.1:p.Asn837Ile
XM_017000852.1:c.3488A>T	XP_016856341.1:p.Asn1163Ile
NM_201253.3:c.3353A>T MANE Select	NP_957705.1:p.Asn1118Ile
NM_001193640.2:c.3017A>T	NP_001180569.1:p.Asn1006Ile
NM_001257965.2:c.3281A>T	NP_001244894.1:p.Asn1094Ile
NR_047563.2:n.3306A>T
NR_047564.2:n.3514A>T
NM_001257966.2:c.2129-384A>T	NP_001244895.1:n.2129-384A>T