Canonical Allele Identifier: CA2670047600

Gene: BOD1L1

Linked Data

• gnomAD v4: 4-13596063-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13596063C>A , CM000666.2:g.13596063C>A	GRCh38
NC_000004.11:g.13597687C>A , CM000666.1:g.13597687C>A	GRCh37
NC_000004.10:g.13206785C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507943.2:c.8020-119G>T	ENSP00000425492.2:n.8020-119G>T
ENST00000040738.10:c.8020-119G>T MANE Select	ENSP00000040738.5:n.8020-119G>T
ENST00000040738.9:c.8020-119G>T	ENSP00000040738.5:n.8020-119G>T
NM_148894.2:c.8020-119G>T	NP_683692.2:n.8020-119G>T
XM_005248150.2:c.8020-119G>T	XP_005248207.1:n.8020-119G>T
XM_005248151.2:c.8020-119G>T	XP_005248208.1:n.8020-119G>T
XM_006713958.2:c.8020-119G>T	XP_006714021.1:n.8020-119G>T
XM_011513827.1:c.8020-119G>T	XP_011512129.1:n.8020-119G>T
XM_011513828.1:c.8020-119G>T	XP_011512130.1:n.8020-119G>T
XM_011513829.1:c.8020-119G>T	XP_011512131.1:n.8020-119G>T
XM_011513830.1:c.7417-119G>T	XP_011512132.1:n.7417-119G>T
XM_005248150.3:c.8020-119G>T	XP_005248207.1:n.8020-119G>T
XM_005248151.3:c.8020-119G>T	XP_005248208.1:n.8020-119G>T
XM_006713958.3:c.8020-119G>T	XP_006714021.1:n.8020-119G>T
XM_011513827.2:c.8020-119G>T	XP_011512129.1:n.8020-119G>T
XM_011513829.2:c.8020-119G>T	XP_011512131.1:n.8020-119G>T
XM_011513830.3:c.7417-119G>T	XP_011512132.1:n.7417-119G>T
XM_017008009.1:c.8020-119G>T	XP_016863498.1:n.8020-119G>T
XM_017008010.1:c.8020-119G>T	XP_016863499.1:n.8020-119G>T
NM_148894.3:c.8020-119G>T MANE Select	NP_683692.2:n.8020-119G>T