Canonical Allele Identifier: CA1864361239
Gene: BICD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718923_92718941delinsGCTGGTGCGGCCCCCGGGA , CM000671.2:g.92718923_92718941delinsGCTGGTGCGGCCCCCGGGA GRCh38
NC_000009.11:g.95481205_95481223delinsGCTGGTGCGGCCCCCGGGA , CM000671.1:g.95481205_95481223delinsGCTGGTGCGGCCCCCGGGA GRCh37
NC_000009.10:g.94521026_94521044delinsGCTGGTGCGGCCCCCGGGA NCBI36
NG_033908.1:g.50861_50879delinsTCCCGGGGGCCGCACCAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1704_1722delinsTCCCGGGGGCCGCACCAGC MANE Select ENSP00000349351.6:p.Ser568=
ENST00000356884.10:c.1704_1722delinsTCCCGGGGGCCGCACCAGC ENSP00000349351.6:p.Ser568=
ENST00000375512.3:c.1704_1722delinsTCCCGGGGGCCGCACCAGC ENSP00000364662.3:p.Ser568=
NM_001003800.1:c.1704_1722delinsTCCCGGGGGCCGCACCAGC NP_001003800.1:p.Ser568=
NM_015250.3:c.1704_1722delinsTCCCGGGGGCCGCACCAGC NP_056065.1:p.Ser568=
XM_017014551.1:c.1785_1803delinsTCCCGGGGGCCGCACCAGC XP_016870040.1:p.Ser595=
NM_001003800.2:c.1704_1722delinsTCCCGGGGGCCGCACCAGC MANE Select NP_001003800.1:p.Ser568=
NM_015250.4:c.1704_1722delinsTCCCGGGGGCCGCACCAGC NP_056065.1:p.Ser568=
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