Canonical Allele Identifier: CA687379721

Gene: BICD1

Linked Data

• dbSNP Id: rs1315541193
• gnomAD v3: 12-32323821-TTAA-T
• gnomAD v4: 12-32323821-TTAA-T
• MyVariant Identifiers: chr12:g.32476756_32476758del (hg19) ; chr12:g.32323822_32323824del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32323826_32323828del , CM000674.2:g.32323826_32323828del	GRCh38
NC_000012.11:g.32476760_32476762del , CM000674.1:g.32476760_32476762del	GRCh37
NC_000012.10:g.32368027_32368029del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000548411.6:c.1006-3635_1006-3633del	ENSP00000446793.1:n.1006-3635_1006-3633del
ENST00000652176.1:c.1006-3635_1006-3633del MANE Select	ENSP00000498700.1:n.1006-3635_1006-3633del
ENST00000281474.9:c.1006-3635_1006-3633del	ENSP00000281474.5:n.1006-3635_1006-3633del
ENST00000395758.3:c.1006-3635_1006-3633del	ENSP00000379107.3:n.1006-3635_1006-3633del
ENST00000548411.5:c.1006-3635_1006-3633del	ENSP00000446793.1:n.1006-3635_1006-3633del
NM_001003398.1:c.1006-3635_1006-3633del	NP_001003398.1:n.1006-3635_1006-3633del
NM_001714.2:c.1006-3635_1006-3633del	NP_001705.2:n.1006-3635_1006-3633del
XM_005253465.2:c.1006-3635_1006-3633del	XP_005253522.1:n.1006-3635_1006-3633del
XM_005253466.2:c.1006-3635_1006-3633del	XP_005253523.1:n.1006-3635_1006-3633del
XM_006719134.2:c.1006-3635_1006-3633del	XP_006719197.1:n.1006-3635_1006-3633del
XM_011520812.1:c.1006-3635_1006-3633del	XP_011519114.1:n.1006-3635_1006-3633del
XM_011520813.1:c.1006-3635_1006-3633del	XP_011519115.1:n.1006-3635_1006-3633del
XM_011520814.1:c.1006-3635_1006-3633del	XP_011519116.1:n.1006-3635_1006-3633del
XM_011520815.1:c.1006-3635_1006-3633del	XP_011519117.1:n.1006-3635_1006-3633del
XM_011520816.1:c.1006-3635_1006-3633del	XP_011519118.1:n.1006-3635_1006-3633del
XR_242898.2:n.1602-3635_1602-3633del
NM_001003398.2:c.1006-3635_1006-3633del	NP_001003398.1:n.1006-3635_1006-3633del
NM_001354186.1:c.1006-3635_1006-3633del	NP_001341115.1:n.1006-3635_1006-3633del
NM_001354187.1:c.1006-3635_1006-3633del	NP_001341116.1:n.1006-3635_1006-3633del
NM_001354188.1:c.1006-3635_1006-3633del	NP_001341117.1:n.1006-3635_1006-3633del
NM_001354189.1:c.1006-3635_1006-3633del	NP_001341118.1:n.1006-3635_1006-3633del
NM_001363603.1:c.1006-3635_1006-3633del	NP_001350532.1:n.1006-3635_1006-3633del
NM_001714.3:c.1006-3635_1006-3633del	NP_001705.2:n.1006-3635_1006-3633del
NR_148725.1:n.1531-3635_1531-3633del
XM_011520812.3:c.1006-3635_1006-3633del	XP_011519114.1:n.1006-3635_1006-3633del
XM_011520813.2:c.1006-3635_1006-3633del	XP_011519115.1:n.1006-3635_1006-3633del
XM_011520814.3:c.1006-3635_1006-3633del	XP_011519116.1:n.1006-3635_1006-3633del
XM_011520815.3:c.1006-3635_1006-3633del	XP_011519117.1:n.1006-3635_1006-3633del
XR_002957369.1:n.1565-3635_1565-3633del
NM_001714.4:c.1006-3635_1006-3633del MANE Select	NP_001705.2:n.1006-3635_1006-3633del
NM_001003398.3:c.1006-3635_1006-3633del	NP_001003398.1:n.1006-3635_1006-3633del
NM_001354186.2:c.1006-3635_1006-3633del	NP_001341115.1:n.1006-3635_1006-3633del
NM_001354187.2:c.1006-3635_1006-3633del	NP_001341116.1:n.1006-3635_1006-3633del
NM_001354188.2:c.1006-3635_1006-3633del	NP_001341117.1:n.1006-3635_1006-3633del
NM_001354189.2:c.1006-3635_1006-3633del	NP_001341118.1:n.1006-3635_1006-3633del
NR_148725.2:n.1491-3635_1491-3633del
NM_001363603.2:c.1006-3635_1006-3633del	NP_001350532.1:n.1006-3635_1006-3633del