Canonical Allele Identifier: CA344032946
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421762A>C , CM000663.2:g.197421762A>C GRCh38
NC_000001.10:g.197390892A>C , CM000663.1:g.197390892A>C GRCh37
NC_000001.9:g.195657515A>C NCBI36
NG_008483.1:g.158485A>C
NG_008483.2:g.225301A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1934A>C MANE Select ENSP00000356370.3:p.Asp645Ala
ENST00000638467.1:c.1934A>C ENSP00000491102.1:p.Asp645Ala
ENST00000681519.1:c.815A>C ENSP00000505267.1:p.Asp272Ala
ENST00000367397.1:c.77A>C ENSP00000356367.1:p.Asp26Ala
ENST00000367399.6:c.1598A>C ENSP00000356369.2:p.Asp533Ala
ENST00000367400.7:c.1934A>C ENSP00000356370.3:p.Asp645Ala
ENST00000484075.5:c.1934A>C ENSP00000433932.1:p.Asp645Ala
ENST00000535699.5:c.1727A>C ENSP00000438786.1:p.Asp576Ala
ENST00000538660.5:c.1934A>C ENSP00000438091.1:p.Asp645Ala
NM_001193640.1:c.1598A>C NP_001180569.1:p.Asp533Ala
NM_001257965.1:c.1727A>C NP_001244894.1:p.Asp576Ala
NM_001257966.1:c.1934A>C NP_001244895.1:p.Asp645Ala
NM_201253.2:c.1934A>C NP_957705.1:p.Asp645Ala
NR_047563.1:n.1935A>C
NR_047564.1:n.2143A>C
XM_011509365.1:c.1934A>C XP_011507667.1:p.Asp645Ala
XM_011509366.1:c.1934A>C XP_011507668.1:p.Asp645Ala
XM_011509367.1:c.1934A>C XP_011507669.1:p.Asp645Ala
XM_011509368.1:c.1352A>C XP_011507670.1:p.Asp451Ala
XM_011509369.1:c.377A>C XP_011507671.1:p.Asp126Ala
XM_011509365.2:c.1934A>C XP_011507667.1:p.Asp645Ala
XM_011509369.2:c.377A>C XP_011507671.1:p.Asp126Ala
XM_017000851.1:c.1091A>C XP_016856340.1:p.Asp364Ala
XM_017000852.1:c.1934A>C XP_016856341.1:p.Asp645Ala
NM_201253.3:c.1934A>C MANE Select NP_957705.1:p.Asp645Ala
NM_001193640.2:c.1598A>C NP_001180569.1:p.Asp533Ala
NM_001257965.2:c.1727A>C NP_001244894.1:p.Asp576Ala
NR_047563.2:n.1887A>C
NR_047564.2:n.2095A>C
NM_001257966.2:c.1934A>C NP_001244895.1:p.Asp645Ala