Canonical Allele Identifier: CA342061

Gene: CRLF1

Linked Data

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

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?