Canonical Allele Identifier: CA404850565
Gene: CRLF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18596690T>G , CM000681.2:g.18596690T>G GRCh38
NC_000019.9:g.18707500T>G , CM000681.1:g.18707500T>G GRCh37
NC_000019.8:g.18568500T>G NCBI36
NG_013370.1:g.15161A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.956A>C ENSP00000506849.1:p.Tyr319Ser
ENST00000392386.8:c.956A>C MANE Select ENSP00000376188.2:p.Tyr319Ser
ENST00000392386.7:c.956A>C ENSP00000376188.2:p.Tyr319Ser
ENST00000597131.1:c.421A>C
NM_004750.4:c.956A>C NP_004741.1:p.Tyr319Ser
XM_011528422.1:c.890A>C XP_011526724.1:p.Tyr297Ser
XM_011528423.1:c.956A>C XP_011526725.1:p.Tyr319Ser
XM_011528424.1:c.890A>C XP_011526726.1:p.Tyr297Ser
XM_011528422.2:c.890A>C XP_011526724.1:p.Tyr297Ser
XM_011528423.2:c.956A>C XP_011526725.1:p.Tyr319Ser
XM_011528424.3:c.890A>C XP_011526726.1:p.Tyr297Ser
NM_004750.5:c.956A>C MANE Select NP_004741.1:p.Tyr319Ser