Canonical Allele Identifier: CA2840612142
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719119dup , CM000671.2:g.92719119dup GRCh38
NC_000009.11:g.95481401dup , CM000671.1:g.95481401dup GRCh37
NC_000009.10:g.94521222dup NCBI36
NG_033908.1:g.50683dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1526dup MANE Select ENSP00000349351.6:p.Ser510GlufsTer17
ENST00000356884.10:c.1526dup ENSP00000349351.6:p.Ser510GlufsTer17
ENST00000375512.3:c.1526dup ENSP00000364662.3:p.Ser510GlufsTer17
NM_001003800.1:c.1526dup NP_001003800.1:p.Ser510GlufsTer17
NM_015250.3:c.1526dup NP_056065.1:p.Ser510GlufsTer17
XM_017014551.1:c.1607dup XP_016870040.1:p.Ser537GlufsTer17
NM_001003800.2:c.1526dup MANE Select NP_001003800.1:p.Ser510GlufsTer17
NM_015250.4:c.1526dup NP_056065.1:p.Ser510GlufsTer17