Canonical Allele Identifier: CA404851073
Gene: CRLF1 HGNC NCBI

Linked Data

dbSNP Id: rs201795161

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18597032G>T , CM000681.2:g.18597032G>T GRCh38
NC_000019.9:g.18707842G>T , CM000681.1:g.18707842G>T GRCh37
NC_000019.8:g.18568842G>T NCBI36
NG_013370.1:g.14819C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.715C>A ENSP00000506849.1:p.Pro239Thr
ENST00000392386.8:c.715C>A MANE Select ENSP00000376188.2:p.Pro239Thr
ENST00000392386.7:c.715C>A ENSP00000376188.2:p.Pro239Thr
ENST00000597131.1:c.180C>A
NM_004750.4:c.715C>A NP_004741.1:p.Pro239Thr
XM_011528422.1:c.649C>A XP_011526724.1:p.Pro217Thr
XM_011528423.1:c.715C>A XP_011526725.1:p.Pro239Thr
XM_011528424.1:c.649C>A XP_011526726.1:p.Pro217Thr
XM_011528422.2:c.649C>A XP_011526724.1:p.Pro217Thr
XM_011528423.2:c.715C>A XP_011526725.1:p.Pro239Thr
XM_011528424.3:c.649C>A XP_011526726.1:p.Pro217Thr
NM_004750.5:c.715C>A MANE Select NP_004741.1:p.Pro239Thr