Canonical Allele Identifier: CA1864361103
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718887_92718890delinsTAGG , CM000671.2:g.92718887_92718890delinsTAGG GRCh38
NC_000009.11:g.95481169_95481172delinsTAGG , CM000671.1:g.95481169_95481172delinsTAGG GRCh37
NC_000009.10:g.94520990_94520993delinsTAGG NCBI36
NG_033908.1:g.50912_50915delinsCCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1755_1758delinsCCTA MANE Select ENSP00000349351.6:p.Leu585=
ENST00000356884.10:c.1755_1758delinsCCTA ENSP00000349351.6:p.Leu585=
ENST00000375512.3:c.1755_1758delinsCCTA ENSP00000364662.3:p.Leu585=
NM_001003800.1:c.1755_1758delinsCCTA NP_001003800.1:p.Leu585=
NM_015250.3:c.1755_1758delinsCCTA NP_056065.1:p.Leu585=
XM_017014551.1:c.1836_1839delinsCCTA XP_016870040.1:p.Leu612=
NM_001003800.2:c.1755_1758delinsCCTA MANE Select NP_001003800.1:p.Leu585=
NM_015250.4:c.1755_1758delinsCCTA NP_056065.1:p.Leu585=