Canonical Allele Identifier: CA920074368
Gene: CRLF1 HGNC NCBI

Linked Data

dbSNP Id: rs1600650694

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18596543dup , CM000681.2:g.18596543dup GRCh38
NC_000019.9:g.18707353dup , CM000681.1:g.18707353dup GRCh37
NC_000019.8:g.18568353dup NCBI36
NG_013370.1:g.15308dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.1024+79dup ENSP00000506849.1:n.1024+79dup
ENST00000392386.8:c.1024+79dup MANE Select ENSP00000376188.2:n.1024+79dup
ENST00000392386.7:c.1024+79dup ENSP00000376188.2:n.1024+79dup
ENST00000597131.1:c.447+121dup
NM_004750.4:c.1024+79dup NP_004741.1:n.1024+79dup
XM_011528422.1:c.958+79dup XP_011526724.1:n.958+79dup
XM_011528423.1:c.1024+79dup XP_011526725.1:n.1024+79dup
XM_011528424.1:c.958+79dup XP_011526726.1:n.958+79dup
XM_011528422.2:c.958+79dup XP_011526724.1:n.958+79dup
XM_011528423.2:c.1024+79dup XP_011526725.1:n.1024+79dup
XM_011528424.3:c.958+79dup XP_011526726.1:n.958+79dup
NM_004750.5:c.1024+79dup MANE Select NP_004741.1:n.1024+79dup