Canonical Allele Identifier: CA2690686268

Gene: BICD2

Linked Data

• gnomAD v4: 9-92718960-C-CCCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718961_92718964dup , CM000671.2:g.92718961_92718964dup	GRCh38
NC_000009.11:g.95481243_95481246dup , CM000671.1:g.95481243_95481246dup	GRCh37
NC_000009.10:g.94521064_94521067dup	NCBI36
NG_033908.1:g.50838_50841dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1681_1684dup MANE Select	ENSP00000349351.6:p.Gly562AlafsTer?
ENST00000356884.10:c.1681_1684dup	ENSP00000349351.6:p.Gly562AlafsTer?
ENST00000375512.3:c.1681_1684dup	ENSP00000364662.3:p.Gly562AlafsTer?
NM_001003800.1:c.1681_1684dup	NP_001003800.1:p.Gly562AlafsTer?
NM_015250.3:c.1681_1684dup	NP_056065.1:p.Gly562AlafsTer?
XM_017014551.1:c.1762_1765dup	XP_016870040.1:p.Gly589AlafsTer?
NM_001003800.2:c.1681_1684dup MANE Select	NP_001003800.1:p.Gly562AlafsTer?
NM_015250.4:c.1681_1684dup	NP_056065.1:p.Gly562AlafsTer?