Canonical Allele Identifier: CA404852291
Gene: CRLF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599817T>C , CM000681.2:g.18599817T>C GRCh38
NC_000019.9:g.18710627T>C , CM000681.1:g.18710627T>C GRCh37
NC_000019.8:g.18571627T>C NCBI36
NG_013370.1:g.12034A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.145A>G ENSP00000506849.1:p.Thr49Ala
ENST00000392386.8:c.145A>G MANE Select ENSP00000376188.2:p.Thr49Ala
ENST00000392386.7:c.145A>G ENSP00000376188.2:p.Thr49Ala
ENST00000593286.1:n.397A>G
NM_004750.4:c.145A>G NP_004741.1:p.Thr49Ala
XM_011528422.1:c.79A>G XP_011526724.1:p.Thr27Ala
XM_011528423.1:c.145A>G XP_011526725.1:p.Thr49Ala
XM_011528424.1:c.79A>G XP_011526726.1:p.Thr27Ala
XM_011528422.2:c.79A>G XP_011526724.1:p.Thr27Ala
XM_011528423.2:c.145A>G XP_011526725.1:p.Thr49Ala
XM_011528424.3:c.79A>G XP_011526726.1:p.Thr27Ala
NM_004750.5:c.145A>G MANE Select NP_004741.1:p.Thr49Ala