Canonical Allele Identifier: CA2690686267
Gene: BICD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718958del , CM000671.2:g.92718958del GRCh38
NC_000009.11:g.95481240del , CM000671.1:g.95481240del GRCh37
NC_000009.10:g.94521061del NCBI36
NG_033908.1:g.50847del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1690del MANE Select ENSP00000349351.6:p.Ala564ProfsTer?
ENST00000356884.10:c.1690del ENSP00000349351.6:p.Ala564ProfsTer?
ENST00000375512.3:c.1690del ENSP00000364662.3:p.Ala564ProfsTer?
NM_001003800.1:c.1690del NP_001003800.1:p.Ala564ProfsTer?
NM_015250.3:c.1690del NP_056065.1:p.Ala564ProfsTer?
XM_017014551.1:c.1771del XP_016870040.1:p.Ala591ProfsTer?
NM_001003800.2:c.1690del MANE Select NP_001003800.1:p.Ala564ProfsTer?
NM_015250.4:c.1690del NP_056065.1:p.Ala564ProfsTer?