Canonical Allele Identifier: CA2507569484

Gene: BOD1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13596065_13596066insCG , CM000666.2:g.13596065_13596066insCG	GRCh38
NC_000004.11:g.13597689_13597690insCG , CM000666.1:g.13597689_13597690insCG	GRCh37
NC_000004.10:g.13206787_13206788insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507943.2:c.8020-122_8020-121insCG	ENSP00000425492.2:n.8020-122_8020-121insCG
ENST00000040738.10:c.8020-122_8020-121insCG MANE Select	ENSP00000040738.5:n.8020-122_8020-121insCG
ENST00000040738.9:c.8020-122_8020-121insCG	ENSP00000040738.5:n.8020-122_8020-121insCG
NM_148894.2:c.8020-122_8020-121insCG	NP_683692.2:n.8020-122_8020-121insCG
XM_005248150.2:c.8020-122_8020-121insCG	XP_005248207.1:n.8020-122_8020-121insCG
XM_005248151.2:c.8020-122_8020-121insCG	XP_005248208.1:n.8020-122_8020-121insCG
XM_006713958.2:c.8020-122_8020-121insCG	XP_006714021.1:n.8020-122_8020-121insCG
XM_011513827.1:c.8020-122_8020-121insCG	XP_011512129.1:n.8020-122_8020-121insCG
XM_011513828.1:c.8020-122_8020-121insCG	XP_011512130.1:n.8020-122_8020-121insCG
XM_011513829.1:c.8020-122_8020-121insCG	XP_011512131.1:n.8020-122_8020-121insCG
XM_011513830.1:c.7417-122_7417-121insCG	XP_011512132.1:n.7417-122_7417-121insCG
XM_005248150.3:c.8020-122_8020-121insCG	XP_005248207.1:n.8020-122_8020-121insCG
XM_005248151.3:c.8020-122_8020-121insCG	XP_005248208.1:n.8020-122_8020-121insCG
XM_006713958.3:c.8020-122_8020-121insCG	XP_006714021.1:n.8020-122_8020-121insCG
XM_011513827.2:c.8020-122_8020-121insCG	XP_011512129.1:n.8020-122_8020-121insCG
XM_011513829.2:c.8020-122_8020-121insCG	XP_011512131.1:n.8020-122_8020-121insCG
XM_011513830.3:c.7417-122_7417-121insCG	XP_011512132.1:n.7417-122_7417-121insCG
XM_017008009.1:c.8020-122_8020-121insCG	XP_016863498.1:n.8020-122_8020-121insCG
XM_017008010.1:c.8020-122_8020-121insCG	XP_016863499.1:n.8020-122_8020-121insCG
NM_148894.3:c.8020-122_8020-121insCG MANE Select	NP_683692.2:n.8020-122_8020-121insCG