Canonical Allele Identifier: CA1864362506
Gene: BICD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719486_92719489delinsCCTT , CM000671.2:g.92719486_92719489delinsCCTT GRCh38
NC_000009.11:g.95481768_95481771delinsCCTT , CM000671.1:g.95481768_95481771delinsCCTT GRCh37
NC_000009.10:g.94521589_94521592delinsCCTT NCBI36
NG_033908.1:g.50313_50316delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1156_1159delinsAAGG MANE Select ENSP00000349351.6:p.Lys386=
ENST00000356884.10:c.1156_1159delinsAAGG ENSP00000349351.6:p.Lys386=
ENST00000375512.3:c.1156_1159delinsAAGG ENSP00000364662.3:p.Lys386=
NM_001003800.1:c.1156_1159delinsAAGG NP_001003800.1:p.Lys386=
NM_015250.3:c.1156_1159delinsAAGG NP_056065.1:p.Lys386=
XM_017014551.1:c.1237_1240delinsAAGG XP_016870040.1:p.Lys413=
NM_001003800.2:c.1156_1159delinsAAGG MANE Select NP_001003800.1:p.Lys386=
NM_015250.4:c.1156_1159delinsAAGG NP_056065.1:p.Lys386=
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