Canonical Allele Identifier: CA1864360979
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718840_92718841delinsGT , CM000671.2:g.92718840_92718841delinsGT GRCh38
NC_000009.11:g.95481122_95481123delinsGT , CM000671.1:g.95481122_95481123delinsGT GRCh37
NC_000009.10:g.94520943_94520944delinsGT NCBI36
NG_033908.1:g.50961_50962delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1804_1805delinsAC MANE Select ENSP00000349351.6:p.Thr602=
ENST00000356884.10:c.1804_1805delinsAC ENSP00000349351.6:p.Thr602=
ENST00000375512.3:c.1804_1805delinsAC ENSP00000364662.3:p.Thr602=
NM_001003800.1:c.1804_1805delinsAC NP_001003800.1:p.Thr602=
NM_015250.3:c.1804_1805delinsAC NP_056065.1:p.Thr602=
XM_017014551.1:c.1885_1886delinsAC XP_016870040.1:p.Thr629=
NM_001003800.2:c.1804_1805delinsAC MANE Select NP_001003800.1:p.Thr602=
NM_015250.4:c.1804_1805delinsAC NP_056065.1:p.Thr602=