Canonical Allele Identifier: CA1864362306
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719402_92719405delinsCCTT , CM000671.2:g.92719402_92719405delinsCCTT GRCh38
NC_000009.11:g.95481684_95481687delinsCCTT , CM000671.1:g.95481684_95481687delinsCCTT GRCh37
NC_000009.10:g.94521505_94521508delinsCCTT NCBI36
NG_033908.1:g.50397_50400delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1240_1243delinsAAGG MANE Select ENSP00000349351.6:p.Lys414=
ENST00000356884.10:c.1240_1243delinsAAGG ENSP00000349351.6:p.Lys414=
ENST00000375512.3:c.1240_1243delinsAAGG ENSP00000364662.3:p.Lys414=
NM_001003800.1:c.1240_1243delinsAAGG NP_001003800.1:p.Lys414=
NM_015250.3:c.1240_1243delinsAAGG NP_056065.1:p.Lys414=
XM_017014551.1:c.1321_1324delinsAAGG XP_016870040.1:p.Lys441=
NM_001003800.2:c.1240_1243delinsAAGG MANE Select NP_001003800.1:p.Lys414=
NM_015250.4:c.1240_1243delinsAAGG NP_056065.1:p.Lys414=