Canonical Allele Identifier: CA2579381918
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718937dup , CM000671.2:g.92718937dup GRCh38
NC_000009.11:g.95481219dup , CM000671.1:g.95481219dup GRCh37
NC_000009.10:g.94521040dup NCBI36
NG_033908.1:g.50869dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1712dup MANE Select ENSP00000349351.6:p.Arg572ProfsTer23
ENST00000356884.10:c.1712dup ENSP00000349351.6:p.Arg572ProfsTer23
ENST00000375512.3:c.1712dup ENSP00000364662.3:p.Arg572ProfsTer23
NM_001003800.1:c.1712dup NP_001003800.1:p.Arg572ProfsTer23
NM_015250.3:c.1712dup NP_056065.1:p.Arg572ProfsTer23
XM_017014551.1:c.1793dup XP_016870040.1:p.Arg599ProfsTer23
NM_001003800.2:c.1712dup MANE Select NP_001003800.1:p.Arg572ProfsTer23
NM_015250.4:c.1712dup NP_056065.1:p.Arg572ProfsTer23