Canonical Allele Identifier: CA422808179
Gene: CRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.197390242T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421112T>G , CM000663.2:g.197421112T>G GRCh38
NC_000001.10:g.197390242T>G , CM000663.1:g.197390242T>G GRCh37
NC_000001.9:g.195656865T>G NCBI36
NG_008483.1:g.157835T>G
NG_008483.2:g.224651T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1284T>G MANE Select ENSP00000356370.3:p.Leu428=
ENST00000638467.1:c.1284T>G ENSP00000491102.1:p.Leu428=
ENST00000681519.1:c.165T>G ENSP00000505267.1:p.Leu55=
ENST00000367397.1:c.-574T>G ENSP00000356367.1:n.-574T>G
ENST00000367399.6:c.948T>G ENSP00000356369.2:p.Leu316=
ENST00000367400.7:c.1284T>G ENSP00000356370.3:p.Leu428=
ENST00000476483.1:n.244T>G
ENST00000484075.5:c.1284T>G ENSP00000433932.1:p.Leu428=
ENST00000535699.5:c.1077T>G ENSP00000438786.1:p.Leu359=
ENST00000538660.5:c.1284T>G ENSP00000438091.1:p.Leu428=
NM_001193640.1:c.948T>G NP_001180569.1:p.Leu316=
NM_001257965.1:c.1077T>G NP_001244894.1:p.Leu359=
NM_001257966.1:c.1284T>G NP_001244895.1:p.Leu428=
NM_201253.2:c.1284T>G NP_957705.1:p.Leu428=
NR_047563.1:n.1493T>G
NR_047564.1:n.1493T>G
XM_011509365.1:c.1284T>G XP_011507667.1:p.Leu428=
XM_011509366.1:c.1284T>G XP_011507668.1:p.Leu428=
XM_011509367.1:c.1284T>G XP_011507669.1:p.Leu428=
XM_011509368.1:c.702T>G XP_011507670.1:p.Leu234=
XM_011509369.1:c.-274T>G XP_011507671.1:n.-274T>G
XM_011509365.2:c.1284T>G XP_011507667.1:p.Leu428=
XM_011509369.2:c.-274T>G XP_011507671.1:n.-274T>G
XM_017000851.1:c.441T>G XP_016856340.1:p.Leu147=
XM_017000852.1:c.1284T>G XP_016856341.1:p.Leu428=
NM_201253.3:c.1284T>G MANE Select NP_957705.1:p.Leu428=
NM_001193640.2:c.948T>G NP_001180569.1:p.Leu316=
NM_001257965.2:c.1077T>G NP_001244894.1:p.Leu359=
NR_047563.2:n.1445T>G
NR_047564.2:n.1445T>G
NM_001257966.2:c.1284T>G NP_001244895.1:p.Leu428=