Canonical Allele Identifier: CA1864362316
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719408_92719411delinsCGTT , CM000671.2:g.92719408_92719411delinsCGTT GRCh38
NC_000009.11:g.95481690_95481693delinsCGTT , CM000671.1:g.95481690_95481693delinsCGTT GRCh37
NC_000009.10:g.94521511_94521514delinsCGTT NCBI36
NG_033908.1:g.50391_50394delinsAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1234_1237delinsAACG MANE Select ENSP00000349351.6:p.Asn412=
ENST00000356884.10:c.1234_1237delinsAACG ENSP00000349351.6:p.Asn412=
ENST00000375512.3:c.1234_1237delinsAACG ENSP00000364662.3:p.Asn412=
NM_001003800.1:c.1234_1237delinsAACG NP_001003800.1:p.Asn412=
NM_015250.3:c.1234_1237delinsAACG NP_056065.1:p.Asn412=
XM_017014551.1:c.1315_1318delinsAACG XP_016870040.1:p.Asn439=
NM_001003800.2:c.1234_1237delinsAACG MANE Select NP_001003800.1:p.Asn412=
NM_015250.4:c.1234_1237delinsAACG NP_056065.1:p.Asn412=