Canonical Allele Identifier: CA1864361185
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718912_92718913delinsCG , CM000671.2:g.92718912_92718913delinsCG GRCh38
NC_000009.11:g.95481194_95481195delinsCG , CM000671.1:g.95481194_95481195delinsCG GRCh37
NC_000009.10:g.94521015_94521016delinsCG NCBI36
NG_033908.1:g.50889_50890delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1732_1733delinsCG MANE Select ENSP00000349351.6:p.Arg578=
ENST00000356884.10:c.1732_1733delinsCG ENSP00000349351.6:p.Arg578=
ENST00000375512.3:c.1732_1733delinsCG ENSP00000364662.3:p.Arg578=
NM_001003800.1:c.1732_1733delinsCG NP_001003800.1:p.Arg578=
NM_015250.3:c.1732_1733delinsCG NP_056065.1:p.Arg578=
XM_017014551.1:c.1813_1814delinsCG XP_016870040.1:p.Arg605=
NM_001003800.2:c.1732_1733delinsCG MANE Select NP_001003800.1:p.Arg578=
NM_015250.4:c.1732_1733delinsCG NP_056065.1:p.Arg578=