Canonical Allele Identifier: CA1864360493

Gene: BICD2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718592T= , CM000671.2:g.92718592T=	GRCh38
NC_000009.11:g.95480874T= , CM000671.1:g.95480874T=	GRCh37
NC_000009.10:g.94520695T=	NCBI36
NG_033908.1:g.51210A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.2053A= MANE Select	ENSP00000349351.6:p.Thr685=
ENST00000356884.10:c.2053A=	ENSP00000349351.6:p.Thr685=
ENST00000375512.3:c.2053A=	ENSP00000364662.3:p.Thr685=
NM_001003800.1:c.2053A=	NP_001003800.1:p.Thr685=
NM_015250.3:c.2053A=	NP_056065.1:p.Thr685=
XM_017014551.1:c.2134A=	XP_016870040.1:p.Thr712=
NM_001003800.2:c.2053A= MANE Select	NP_001003800.1:p.Thr685=
NM_015250.4:c.2053A=	NP_056065.1:p.Thr685=