Canonical Allele Identifier: CA1304258624

Gene: COBLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.164684290T= , CM000664.2:g.164684290T=	GRCh38
NC_000002.11:g.165540800T= , CM000664.1:g.165540800T=	GRCh37
NC_000002.10:g.165249046T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652658.2:c.*1656A= MANE Select	ENSP00000498242.1:n.*1656A=
ENST00000375458.6:c.*1656A=	ENSP00000364607.2:n.*1656A=
ENST00000392717.6:c.*1656A=	ENSP00000376478.2:n.*1656A=
ENST00000495084.1:n.126+7931A=
NM_001278458.1:c.*1656A=	NP_001265387.1:n.*1656A=
NM_001278460.1:c.*1656A=	NP_001265389.1:n.*1656A=
NM_001278461.1:c.*1656A=	NP_001265390.1:n.*1656A=
NM_014900.4:c.*1656A=	NP_055715.3:n.*1656A=
NM_001365670.1:c.*1656A=	NP_001352599.1:n.*1656A=
NM_001365671.1:c.3477+7931A=	NP_001352600.1:n.3477+7931A=
NM_001365672.1:c.*1656A=	NP_001352601.1:n.*1656A=
NM_001365673.1:c.*1656A=	NP_001352602.1:n.*1656A=
NM_001365674.1:c.*1656A=	NP_001352603.1:n.*1656A=
NM_001365675.1:c.*1656A=	NP_001352604.1:n.*1656A=
NM_001278458.2:c.*1656A=	NP_001265387.1:n.*1656A=
NM_001278460.2:c.*1656A=	NP_001265389.1:n.*1656A=
NM_001278461.2:c.*1656A=	NP_001265390.1:n.*1656A=
NM_001365670.2:c.*1656A=	NP_001352599.1:n.*1656A=
NM_001365672.2:c.*1656A= MANE Select	NP_001352601.1:n.*1656A=
NM_001365673.2:c.*1656A=	NP_001352602.1:n.*1656A=
NM_001365674.2:c.*1656A=	NP_001352603.1:n.*1656A=
NM_001365675.2:c.*1656A=	NP_001352604.1:n.*1656A=
NM_014900.5:c.*1656A=	NP_055715.3:n.*1656A=