Canonical Allele Identifier: CA1864362453
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1853412106

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719471_92719472del , CM000671.2:g.92719471_92719472del GRCh38
NC_000009.11:g.95481753_95481754del , CM000671.1:g.95481753_95481754del GRCh37
NC_000009.10:g.94521574_94521575del NCBI36
NG_033908.1:g.50333_50334del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1176_1177del MANE Select ENSP00000349351.6:p.Asn393SerfsTer24
ENST00000356884.10:c.1176_1177del ENSP00000349351.6:p.Asn393SerfsTer24
ENST00000375512.3:c.1176_1177del ENSP00000364662.3:p.Asn393SerfsTer24
NM_001003800.1:c.1176_1177del NP_001003800.1:p.Asn393SerfsTer24
NM_015250.3:c.1176_1177del NP_056065.1:p.Asn393SerfsTer24
XM_017014551.1:c.1257_1258del XP_016870040.1:p.Asn420SerfsTer24
NM_001003800.2:c.1176_1177del MANE Select NP_001003800.1:p.Asn393SerfsTer24
NM_015250.4:c.1176_1177del NP_056065.1:p.Asn393SerfsTer24