Canonical Allele Identifier: CA235200128

Gene: BICD1

Linked Data

• dbSNP Id: rs10844154
• MyVariant Identifiers: chr12:g.32380501A>T (hg19) ; chr12:g.32227567A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32227567A>T , CM000674.2:g.32227567A>T	GRCh38
NC_000012.11:g.32380501A>T , CM000674.1:g.32380501A>T	GRCh37
NC_000012.10:g.32271768A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000548411.6:c.426+11108A>T	ENSP00000446793.1:n.426+11108A>T
ENST00000652176.1:c.426+11108A>T MANE Select	ENSP00000498700.1:n.426+11108A>T
ENST00000281474.9:c.426+11108A>T	ENSP00000281474.5:n.426+11108A>T
ENST00000395758.3:c.426+11108A>T	ENSP00000379107.3:n.426+11108A>T
ENST00000548411.5:c.426+11108A>T	ENSP00000446793.1:n.426+11108A>T
ENST00000549976.1:n.588T>A
NM_001003398.1:c.426+11108A>T	NP_001003398.1:n.426+11108A>T
NM_001714.2:c.426+11108A>T	NP_001705.2:n.426+11108A>T
XM_005253465.2:c.426+11108A>T	XP_005253522.1:n.426+11108A>T
XM_005253466.2:c.426+11108A>T	XP_005253523.1:n.426+11108A>T
XM_006719134.2:c.426+11108A>T	XP_006719197.1:n.426+11108A>T
XM_011520812.1:c.426+11108A>T	XP_011519114.1:n.426+11108A>T
XM_011520813.1:c.426+11108A>T	XP_011519115.1:n.426+11108A>T
XM_011520814.1:c.426+11108A>T	XP_011519116.1:n.426+11108A>T
XM_011520815.1:c.426+11108A>T	XP_011519117.1:n.426+11108A>T
XM_011520816.1:c.426+11108A>T	XP_011519118.1:n.426+11108A>T
XR_242898.2:n.1022+11108A>T
NM_001003398.2:c.426+11108A>T	NP_001003398.1:n.426+11108A>T
NM_001354186.1:c.426+11108A>T	NP_001341115.1:n.426+11108A>T
NM_001354187.1:c.426+11108A>T	NP_001341116.1:n.426+11108A>T
NM_001354188.1:c.426+11108A>T	NP_001341117.1:n.426+11108A>T
NM_001354189.1:c.426+11108A>T	NP_001341118.1:n.426+11108A>T
NM_001363603.1:c.426+11108A>T	NP_001350532.1:n.426+11108A>T
NM_001714.3:c.426+11108A>T	NP_001705.2:n.426+11108A>T
NR_148725.1:n.951+11108A>T
XM_011520812.3:c.426+11108A>T	XP_011519114.1:n.426+11108A>T
XM_011520813.2:c.426+11108A>T	XP_011519115.1:n.426+11108A>T
XM_011520814.3:c.426+11108A>T	XP_011519116.1:n.426+11108A>T
XM_011520815.3:c.426+11108A>T	XP_011519117.1:n.426+11108A>T
XR_002957369.1:n.985+11108A>T
NM_001714.4:c.426+11108A>T MANE Select	NP_001705.2:n.426+11108A>T
NM_001003398.3:c.426+11108A>T	NP_001003398.1:n.426+11108A>T
NM_001354186.2:c.426+11108A>T	NP_001341115.1:n.426+11108A>T
NM_001354187.2:c.426+11108A>T	NP_001341116.1:n.426+11108A>T
NM_001354188.2:c.426+11108A>T	NP_001341117.1:n.426+11108A>T
NM_001354189.2:c.426+11108A>T	NP_001341118.1:n.426+11108A>T
NR_148725.2:n.911+11108A>T
NM_001363603.2:c.426+11108A>T	NP_001350532.1:n.426+11108A>T