Canonical Allele Identifier: CA404851098
Gene: CRLF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18597044T>C , CM000681.2:g.18597044T>C GRCh38
NC_000019.9:g.18707854T>C , CM000681.1:g.18707854T>C GRCh37
NC_000019.8:g.18568854T>C NCBI36
NG_013370.1:g.14807A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.703A>G ENSP00000506849.1:p.Thr235Ala
ENST00000392386.8:c.703A>G MANE Select ENSP00000376188.2:p.Thr235Ala
ENST00000392386.7:c.703A>G ENSP00000376188.2:p.Thr235Ala
ENST00000597131.1:c.168A>G
NM_004750.4:c.703A>G NP_004741.1:p.Thr235Ala
XM_011528422.1:c.637A>G XP_011526724.1:p.Thr213Ala
XM_011528423.1:c.703A>G XP_011526725.1:p.Thr235Ala
XM_011528424.1:c.637A>G XP_011526726.1:p.Thr213Ala
XM_011528422.2:c.637A>G XP_011526724.1:p.Thr213Ala
XM_011528423.2:c.703A>G XP_011526725.1:p.Thr235Ala
XM_011528424.3:c.637A>G XP_011526726.1:p.Thr213Ala
NM_004750.5:c.703A>G MANE Select NP_004741.1:p.Thr235Ala