Canonical Allele Identifier: CA915952925

Gene: CRLF1

Linked Data

• ClinVar Variation Id: 816854
• ClinVar RCV Id: RCV001007859
• dbSNP Id: rs1600650861

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596661dup , CM000681.2:g.18596661dup	GRCh38
NC_000019.9:g.18707471dup , CM000681.1:g.18707471dup	GRCh37
NC_000019.8:g.18568471dup	NCBI36
NG_013370.1:g.15190dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.985dup	ENSP00000506849.1:p.Glu329GlyfsTer14
ENST00000392386.8:c.985dup MANE Select	ENSP00000376188.2:p.Glu329GlyfsTer14
ENST00000392386.7:c.985dup	ENSP00000376188.2:p.Glu329GlyfsTer14
ENST00000597131.1:c.447+3dup
NM_004750.4:c.985dup	NP_004741.1:p.Glu329GlyfsTer14
XM_011528422.1:c.919dup	XP_011526724.1:p.Glu307GlyfsTer14
XM_011528423.1:c.985dup	XP_011526725.1:p.Glu329GlyfsTer14
XM_011528424.1:c.919dup	XP_011526726.1:p.Glu307GlyfsTer14
XM_011528422.2:c.919dup	XP_011526724.1:p.Glu307GlyfsTer14
XM_011528423.2:c.985dup	XP_011526725.1:p.Glu329GlyfsTer14
XM_011528424.3:c.919dup	XP_011526726.1:p.Glu307GlyfsTer14
NM_004750.5:c.985dup MANE Select	NP_004741.1:p.Glu329GlyfsTer14