Canonical Allele Identifier: CA2690686274
Gene: BICD2 HGNC NCBI

Linked Data

gnomAD v4: 9-92719489-TCTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719492_92719494del , CM000671.2:g.92719492_92719494del GRCh38
NC_000009.11:g.95481774_95481776del , CM000671.1:g.95481774_95481776del GRCh37
NC_000009.10:g.94521595_94521597del NCBI36
NG_033908.1:g.50310_50312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1153_1155del MANE Select ENSP00000349351.6:p.Glu385del
ENST00000356884.10:c.1153_1155del ENSP00000349351.6:p.Glu385del
ENST00000375512.3:c.1153_1155del ENSP00000364662.3:p.Glu385del
NM_001003800.1:c.1153_1155del NP_001003800.1:p.Glu385del
NM_015250.3:c.1153_1155del NP_056065.1:p.Glu385del
XM_017014551.1:c.1234_1236del XP_016870040.1:p.Glu412del
NM_001003800.2:c.1153_1155del MANE Select NP_001003800.1:p.Glu385del
NM_015250.4:c.1153_1155del NP_056065.1:p.Glu385del
Search 100 bp 5'
Search 100 bp 3'