Canonical Allele Identifier: CA2326432229
Gene: CRLF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18596634T= , CM000681.2:g.18596634T= GRCh38
NC_000019.9:g.18707444T= , CM000681.1:g.18707444T= GRCh37
NC_000019.8:g.18568444T= NCBI36
NG_013370.1:g.15217A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.1012A= ENSP00000506849.1:p.Thr338=
ENST00000392386.8:c.1012A= MANE Select ENSP00000376188.2:p.Thr338=
ENST00000392386.7:c.1012A= ENSP00000376188.2:p.Thr338=
ENST00000597131.1:c.447+30A=
NM_004750.4:c.1012A= NP_004741.1:p.Thr338=
XM_011528422.1:c.946A= XP_011526724.1:p.Thr316=
XM_011528423.1:c.1012A= XP_011526725.1:p.Thr338=
XM_011528424.1:c.946A= XP_011526726.1:p.Thr316=
XM_011528422.2:c.946A= XP_011526724.1:p.Thr316=
XM_011528423.2:c.1012A= XP_011526725.1:p.Thr338=
XM_011528424.3:c.946A= XP_011526726.1:p.Thr316=
NM_004750.5:c.1012A= MANE Select NP_004741.1:p.Thr338=