Canonical Allele Identifier: CA1937191
Gene: COBLL1 HGNC NCBI
COSMIC:
MyVariant.info:
Revel Score:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.164694691T>C , CM000664.2:g.164694691T>C GRCh38
NC_000002.11:g.165551201T>C , CM000664.1:g.165551201T>C GRCh37
NC_000002.10:g.165259447T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000409184.8:c.2839A>G ENSP00000387326.5:p.Asn947Asp
ENST00000652658.2:c.2701A>G MANE Select ENSP00000498242.1:p.Asn901Asp
ENST00000342193.8:c.2815A>G ENSP00000341360.4:p.Asn939Asp
ENST00000375458.6:c.2701A>G ENSP00000364607.2:p.Asn901Asp
ENST00000392717.6:c.2929A>G ENSP00000376478.2:p.Asn977Asp
ENST00000409184.7:c.2820A>G
ENST00000489955.1:n.3610A>G
ENST00000493713.1:n.47A>G
ENST00000493868.5:n.4525A>G
ENST00000629362.2:c.3016A>G ENSP00000487041.2:p.Asn1006Asp
NM_001278458.1:c.3016A>G NP_001265387.1:p.Asn1006Asp
NM_001278460.1:c.2839A>G NP_001265389.1:p.Asn947Asp
NM_001278461.1:c.2701A>G NP_001265390.1:p.Asn901Asp
NM_014900.4:c.2815A>G NP_055715.3:p.Asn939Asp
NM_001365670.1:c.2836A>G NP_001352599.1:p.Asn946Asp
NM_001365671.1:c.2878A>G NP_001352600.1:p.Asn960Asp
NM_001365672.1:c.2701A>G NP_001352601.1:p.Asn901Asp
NM_001365673.1:c.2701A>G NP_001352602.1:p.Asn901Asp
NM_001365674.1:c.2740A>G NP_001352603.1:p.Asn914Asp
NM_001365675.1:c.2740A>G NP_001352604.1:p.Asn914Asp
NM_001278458.2:c.3016A>G NP_001265387.1:p.Asn1006Asp
NM_001278460.2:c.2839A>G NP_001265389.1:p.Asn947Asp
NM_001278461.2:c.2701A>G NP_001265390.1:p.Asn901Asp
NM_001365670.2:c.2836A>G NP_001352599.1:p.Asn946Asp
NM_001365672.2:c.2701A>G MANE Select NP_001352601.1:p.Asn901Asp
NM_001365673.2:c.2701A>G NP_001352602.1:p.Asn901Asp
NM_001365674.2:c.2740A>G NP_001352603.1:p.Asn914Asp
NM_001365675.2:c.2740A>G NP_001352604.1:p.Asn914Asp
NM_014900.5:c.2815A>G NP_055715.3:p.Asn939Asp