Canonical Allele Identifier: CA645547587
Gene: BICD2 HGNC NCBI

Linked Data

COSMIC: COSM5835807 COSM5835808
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719017_92719018insG , CM000671.2:g.92719017_92719018insG GRCh38
NC_000009.11:g.95481299_95481300insG , CM000671.1:g.95481299_95481300insG GRCh37
NC_000009.10:g.94521120_94521121insG NCBI36
NG_033908.1:g.50784_50785insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1627_1628insC MANE Select ENSP00000349351.6:p.Met543ThrfsTer5
ENST00000356884.10:c.1627_1628insC ENSP00000349351.6:p.Met543ThrfsTer5
ENST00000375512.3:c.1627_1628insC ENSP00000364662.3:p.Met543ThrfsTer5
NM_001003800.1:c.1627_1628insC NP_001003800.1:p.Met543ThrfsTer5
NM_015250.3:c.1627_1628insC NP_056065.1:p.Met543ThrfsTer5
XM_017014551.1:c.1708_1709insC XP_016870040.1:p.Met570ThrfsTer5
NM_001003800.2:c.1627_1628insC MANE Select NP_001003800.1:p.Met543ThrfsTer5
NM_015250.4:c.1627_1628insC NP_056065.1:p.Met543ThrfsTer5
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