Canonical Allele Identifier: CA1864360495
Gene: BICD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718593_92718594delinsGC , CM000671.2:g.92718593_92718594delinsGC GRCh38
NC_000009.11:g.95480875_95480876delinsGC , CM000671.1:g.95480875_95480876delinsGC GRCh37
NC_000009.10:g.94520696_94520697delinsGC NCBI36
NG_033908.1:g.51208_51209delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2051_2052delinsGC MANE Select ENSP00000349351.6:p.Ser684=
ENST00000356884.10:c.2051_2052delinsGC ENSP00000349351.6:p.Ser684=
ENST00000375512.3:c.2051_2052delinsGC ENSP00000364662.3:p.Ser684=
NM_001003800.1:c.2051_2052delinsGC NP_001003800.1:p.Ser684=
NM_015250.3:c.2051_2052delinsGC NP_056065.1:p.Ser684=
XM_017014551.1:c.2132_2133delinsGC XP_016870040.1:p.Ser711=
NM_001003800.2:c.2051_2052delinsGC MANE Select NP_001003800.1:p.Ser684=
NM_015250.4:c.2051_2052delinsGC NP_056065.1:p.Ser684=
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