Canonical Allele Identifier: CA2695228416
Gene: CRLF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18597010_18597026dup , CM000681.2:g.18597010_18597026dup GRCh38
NC_000019.9:g.18707820_18707836dup , CM000681.1:g.18707820_18707836dup GRCh37
NC_000019.8:g.18568820_18568836dup NCBI36
NG_013370.1:g.14825_14841dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.721_737dup ENSP00000506849.1:p.Gly247CysfsTer3
ENST00000392386.8:c.721_737dup MANE Select ENSP00000376188.2:p.Gly247CysfsTer3
ENST00000392386.7:c.721_737dup ENSP00000376188.2:p.Gly247CysfsTer3
ENST00000597131.1:c.186_202dup
NM_004750.4:c.721_737dup NP_004741.1:p.Gly247CysfsTer3
XM_011528422.1:c.655_671dup XP_011526724.1:p.Gly225CysfsTer3
XM_011528423.1:c.721_737dup XP_011526725.1:p.Gly247CysfsTer3
XM_011528424.1:c.655_671dup XP_011526726.1:p.Gly225CysfsTer3
XM_011528422.2:c.655_671dup XP_011526724.1:p.Gly225CysfsTer3
XM_011528423.2:c.721_737dup XP_011526725.1:p.Gly247CysfsTer3
XM_011528424.3:c.655_671dup XP_011526726.1:p.Gly225CysfsTer3
NM_004750.5:c.721_737dup MANE Select NP_004741.1:p.Gly247CysfsTer3