Canonical Allele Identifier: CA404850958
Community Standard Title: NM_004750.5(CRLF1):c.776C>A (p.Ser259Ter)
Gene: CRLF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18596971G>T , CM000681.2:g.18596971G>T GRCh38
NC_000019.9:g.18707781G>T , CM000681.1:g.18707781G>T GRCh37
NC_000019.8:g.18568781G>T NCBI36
NG_013370.1:g.14880C>A

Transcript Alleles

HGVS Amino-acid Change
NM_004750.5:c.776C>A MANE Select NP_004741.1:p.Ser259Ter
ENST00000392386.8:c.776C>A MANE Select ENSP00000376188.2:p.Ser259Ter
NM_004750.4:c.776C>A NP_004741.1:p.Ser259Ter
ENST00000392386.7:c.776C>A ENSP00000376188.2:p.Ser259Ter
ENST00000597131.1:c.241C>A
ENST00000684169.1:c.776C>A ENSP00000506849.1:p.Ser259Ter
XM_011528422.1:c.710C>A XP_011526724.1:p.Ser237Ter
XM_011528422.2:c.710C>A XP_011526724.1:p.Ser237Ter
XM_011528423.1:c.776C>A XP_011526725.1:p.Ser259Ter
XM_011528423.2:c.776C>A XP_011526725.1:p.Ser259Ter
XM_011528424.1:c.710C>A XP_011526726.1:p.Ser237Ter
XM_011528424.3:c.710C>A XP_011526726.1:p.Ser237Ter