Canonical Allele Identifier: CA2690686270

Gene: BICD2

Linked Data

• gnomAD v4: 9-92719311-T-TCAGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92719320_92719325dup , CM000671.2:g.92719320_92719325dup	GRCh38
NC_000009.11:g.95481602_95481607dup , CM000671.1:g.95481602_95481607dup	GRCh37
NC_000009.10:g.94521423_94521428dup	NCBI36
NG_033908.1:g.50485_50490dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1328_1333dup MANE Select	ENSP00000349351.6:p.Ala444_Glu445insValAla
ENST00000356884.10:c.1328_1333dup	ENSP00000349351.6:p.Ala444_Glu445insValAla
ENST00000375512.3:c.1328_1333dup	ENSP00000364662.3:p.Ala444_Glu445insValAla
NM_001003800.1:c.1328_1333dup	NP_001003800.1:p.Ala444_Glu445insValAla
NM_015250.3:c.1328_1333dup	NP_056065.1:p.Ala444_Glu445insValAla
XM_017014551.1:c.1409_1414dup	XP_016870040.1:p.Ala471_Glu472insValAla
NM_001003800.2:c.1328_1333dup MANE Select	NP_001003800.1:p.Ala444_Glu445insValAla
NM_015250.4:c.1328_1333dup	NP_056065.1:p.Ala444_Glu445insValAla