Canonical Allele Identifier: CA422808486

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390404C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421274C>A , CM000663.2:g.197421274C>A	GRCh38
NC_000001.10:g.197390404C>A , CM000663.1:g.197390404C>A	GRCh37
NC_000001.9:g.195657027C>A	NCBI36
NG_008483.1:g.157997C>A
NG_008483.2:g.224813C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.1446C>A MANE Select	ENSP00000356370.3:p.Ile482=
ENST00000638467.1:c.1446C>A	ENSP00000491102.1:p.Ile482=
ENST00000681519.1:c.327C>A	ENSP00000505267.1:p.Ile109=
ENST00000367397.1:c.-412C>A	ENSP00000356367.1:n.-412C>A
ENST00000367399.6:c.1110C>A	ENSP00000356369.2:p.Ile370=
ENST00000367400.7:c.1446C>A	ENSP00000356370.3:p.Ile482=
ENST00000476483.1:n.406C>A
ENST00000484075.5:c.1446C>A	ENSP00000433932.1:p.Ile482=
ENST00000535699.5:c.1239C>A	ENSP00000438786.1:p.Ile413=
ENST00000538660.5:c.1446C>A	ENSP00000438091.1:p.Ile482=
NM_001193640.1:c.1110C>A	NP_001180569.1:p.Ile370=
NM_001257965.1:c.1239C>A	NP_001244894.1:p.Ile413=
NM_001257966.1:c.1446C>A	NP_001244895.1:p.Ile482=
NM_201253.2:c.1446C>A	NP_957705.1:p.Ile482=
NR_047563.1:n.1655C>A
NR_047564.1:n.1655C>A
XM_011509365.1:c.1446C>A	XP_011507667.1:p.Ile482=
XM_011509366.1:c.1446C>A	XP_011507668.1:p.Ile482=
XM_011509367.1:c.1446C>A	XP_011507669.1:p.Ile482=
XM_011509368.1:c.864C>A	XP_011507670.1:p.Ile288=
XM_011509369.1:c.-112C>A	XP_011507671.1:n.-112C>A
XM_011509365.2:c.1446C>A	XP_011507667.1:p.Ile482=
XM_011509369.2:c.-112C>A	XP_011507671.1:n.-112C>A
XM_017000851.1:c.603C>A	XP_016856340.1:p.Ile201=
XM_017000852.1:c.1446C>A	XP_016856341.1:p.Ile482=
NM_201253.3:c.1446C>A MANE Select	NP_957705.1:p.Ile482=
NM_001193640.2:c.1110C>A	NP_001180569.1:p.Ile370=
NM_001257965.2:c.1239C>A	NP_001244894.1:p.Ile413=
NR_047563.2:n.1607C>A
NR_047564.2:n.1607C>A
NM_001257966.2:c.1446C>A	NP_001244895.1:p.Ile482=