Canonical Allele Identifier: CA1864360607
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1853378961
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718650_92718651insTTCTCC , CM000671.2:g.92718650_92718651insTTCTCC GRCh38
NC_000009.11:g.95480932_95480933insTTCTCC , CM000671.1:g.95480932_95480933insTTCTCC GRCh37
NC_000009.10:g.94520753_94520754insTTCTCC NCBI36
NG_033908.1:g.51154_51155insGAAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1997_1998insGAAGGA MANE Select ENSP00000349351.6:p.Val665_Asp666insGluLys
ENST00000356884.10:c.1997_1998insGAAGGA ENSP00000349351.6:p.Val665_Asp666insGluLys
ENST00000375512.3:c.1997_1998insGAAGGA ENSP00000364662.3:p.Val665_Asp666insGluLys
NM_001003800.1:c.1997_1998insGAAGGA NP_001003800.1:p.Val665_Asp666insGluLys
NM_015250.3:c.1997_1998insGAAGGA NP_056065.1:p.Val665_Asp666insGluLys
XM_017014551.1:c.2078_2079insGAAGGA XP_016870040.1:p.Val692_Asp693insGluLys
NM_001003800.2:c.1997_1998insGAAGGA MANE Select NP_001003800.1:p.Val665_Asp666insGluLys
NM_015250.4:c.1997_1998insGAAGGA NP_056065.1:p.Val665_Asp666insGluLys
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