Canonical Allele Identifier: CA1864362350

Gene: BICD2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92719423_92719441delinsTCTGCCGCTCCTTGCTGGC , CM000671.2:g.92719423_92719441delinsTCTGCCGCTCCTTGCTGGC	GRCh38
NC_000009.11:g.95481705_95481723delinsTCTGCCGCTCCTTGCTGGC , CM000671.1:g.95481705_95481723delinsTCTGCCGCTCCTTGCTGGC	GRCh37
NC_000009.10:g.94521526_94521544delinsTCTGCCGCTCCTTGCTGGC	NCBI36
NG_033908.1:g.50361_50379delinsGCCAGCAAGGAGCGGCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA MANE Select	ENSP00000349351.6:p.Ala402=
ENST00000356884.10:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA	ENSP00000349351.6:p.Ala402=
ENST00000375512.3:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA	ENSP00000364662.3:p.Ala402=
NM_001003800.1:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA	NP_001003800.1:p.Ala402=
NM_015250.3:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA	NP_056065.1:p.Ala402=
XM_017014551.1:c.1285_1303delinsGCCAGCAAGGAGCGGCAGA	XP_016870040.1:p.Ala429=
NM_001003800.2:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA MANE Select	NP_001003800.1:p.Ala402=
NM_015250.4:c.1204_1222delinsGCCAGCAAGGAGCGGCAGA	NP_056065.1:p.Ala402=