Canonical Allele Identifier: CA2326433890
Gene: CRLF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599787_18599790delinsTGGC , CM000681.2:g.18599787_18599790delinsTGGC GRCh38
NC_000019.9:g.18710597_18710600delinsTGGC , CM000681.1:g.18710597_18710600delinsTGGC GRCh37
NC_000019.8:g.18571597_18571600delinsTGGC NCBI36
NG_013370.1:g.12061_12064delinsGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.172_175delinsGCCA ENSP00000506849.1:p.Ala58=
ENST00000392386.8:c.172_175delinsGCCA MANE Select ENSP00000376188.2:p.Ala58=
ENST00000392386.7:c.172_175delinsGCCA ENSP00000376188.2:p.Ala58=
ENST00000593286.1:n.424_427delinsGCCA
NM_004750.4:c.172_175delinsGCCA NP_004741.1:p.Ala58=
XM_011528422.1:c.106_109delinsGCCA XP_011526724.1:p.Ala36=
XM_011528423.1:c.172_175delinsGCCA XP_011526725.1:p.Ala58=
XM_011528424.1:c.106_109delinsGCCA XP_011526726.1:p.Ala36=
XM_011528422.2:c.106_109delinsGCCA XP_011526724.1:p.Ala36=
XM_011528423.2:c.172_175delinsGCCA XP_011526725.1:p.Ala58=
XM_011528424.3:c.106_109delinsGCCA XP_011526726.1:p.Ala36=
NM_004750.5:c.172_175delinsGCCA MANE Select NP_004741.1:p.Ala58=