Canonical Allele Identifier: CA342061
Gene: CRLF1 HGNC NCBI

Linked Data

dbSNP Id: rs137853931
MyVariant Identifiers: chr19:g.18710469del (hg19) chr19:g.18599659del (hg38)
PubMed: PMID:21370513
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599660del , CM000681.2:g.18599660del GRCh38
NC_000019.9:g.18710470del , CM000681.1:g.18710470del GRCh37
NC_000019.8:g.18571470del NCBI36
NG_013370.1:g.12192del

Transcript Alleles

HGVS Amino-acid change
ENST00000684169.1:c.303del ENSP00000506849.1:p.Asn102ThrfsTer?
ENST00000392386.8:c.303del MANE Select ENSP00000376188.2:p.Asn102ThrfsTer?
ENST00000392386.7:c.303del ENSP00000376188.2:p.Asn102ThrfsTer?
NM_004750.4:c.303del NP_004741.1:p.Asn102ThrfsTer?
XM_011528422.1:c.237del XP_011526724.1:p.Asn80ThrfsTer?
XM_011528423.1:c.303del XP_011526725.1:p.Asn102ThrfsTer?
XM_011528424.1:c.237del XP_011526726.1:p.Asn80ThrfsTer?
XM_011528422.2:c.237del XP_011526724.1:p.Asn80ThrfsTer?
XM_011528423.2:c.303del XP_011526725.1:p.Asn102ThrfsTer?
XM_011528424.3:c.237del XP_011526726.1:p.Asn80ThrfsTer?
NM_004750.5:c.303del MANE Select NP_004741.1:p.Asn102ThrfsTer?
Search 100 bp 5'
Search 100 bp 3'