Canonical Allele Identifier: CA2579381919
Gene: BICD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719464dup , CM000671.2:g.92719464dup GRCh38
NC_000009.11:g.95481746dup , CM000671.1:g.95481746dup GRCh37
NC_000009.10:g.94521567dup NCBI36
NG_033908.1:g.50338dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1181dup MANE Select ENSP00000349351.6:p.Ser395GlufsTer23
ENST00000356884.10:c.1181dup ENSP00000349351.6:p.Ser395GlufsTer23
ENST00000375512.3:c.1181dup ENSP00000364662.3:p.Ser395GlufsTer23
NM_001003800.1:c.1181dup NP_001003800.1:p.Ser395GlufsTer23
NM_015250.3:c.1181dup NP_056065.1:p.Ser395GlufsTer23
XM_017014551.1:c.1262dup XP_016870040.1:p.Ser422GlufsTer23
NM_001003800.2:c.1181dup MANE Select NP_001003800.1:p.Ser395GlufsTer23
NM_015250.4:c.1181dup NP_056065.1:p.Ser395GlufsTer23
Search 100 bp 5'
Search 100 bp 3'