Canonical Allele Identifier: CA1864361457
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719006_92719009delinsCATT , CM000671.2:g.92719006_92719009delinsCATT GRCh38
NC_000009.11:g.95481288_95481291delinsCATT , CM000671.1:g.95481288_95481291delinsCATT GRCh37
NC_000009.10:g.94521109_94521112delinsCATT NCBI36
NG_033908.1:g.50793_50796delinsAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1636_1639delinsAATG MANE Select ENSP00000349351.6:p.Asn546=
ENST00000356884.10:c.1636_1639delinsAATG ENSP00000349351.6:p.Asn546=
ENST00000375512.3:c.1636_1639delinsAATG ENSP00000364662.3:p.Asn546=
NM_001003800.1:c.1636_1639delinsAATG NP_001003800.1:p.Asn546=
NM_015250.3:c.1636_1639delinsAATG NP_056065.1:p.Asn546=
XM_017014551.1:c.1717_1720delinsAATG XP_016870040.1:p.Asn573=
NM_001003800.2:c.1636_1639delinsAATG MANE Select NP_001003800.1:p.Asn546=
NM_015250.4:c.1636_1639delinsAATG NP_056065.1:p.Asn546=