Canonical Allele Identifier: CA2326432242

Gene: CRLF1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596656_18596660delinsCCACT , CM000681.2:g.18596656_18596660delinsCCACT	GRCh38
NC_000019.9:g.18707466_18707470delinsCCACT , CM000681.1:g.18707466_18707470delinsCCACT	GRCh37
NC_000019.8:g.18568466_18568470delinsCCACT	NCBI36
NG_013370.1:g.15191_15195delinsAGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.986_990delinsAGTGG	ENSP00000506849.1:p.Glu329=
ENST00000392386.8:c.986_990delinsAGTGG MANE Select	ENSP00000376188.2:p.Glu329=
ENST00000392386.7:c.986_990delinsAGTGG	ENSP00000376188.2:p.Glu329=
ENST00000597131.1:c.447+4_447+8delinsAGTGG
NM_004750.4:c.986_990delinsAGTGG	NP_004741.1:p.Glu329=
XM_011528422.1:c.920_924delinsAGTGG	XP_011526724.1:p.Glu307=
XM_011528423.1:c.986_990delinsAGTGG	XP_011526725.1:p.Glu329=
XM_011528424.1:c.920_924delinsAGTGG	XP_011526726.1:p.Glu307=
XM_011528422.2:c.920_924delinsAGTGG	XP_011526724.1:p.Glu307=
XM_011528423.2:c.986_990delinsAGTGG	XP_011526725.1:p.Glu329=
XM_011528424.3:c.920_924delinsAGTGG	XP_011526726.1:p.Glu307=
NM_004750.5:c.986_990delinsAGTGG MANE Select	NP_004741.1:p.Glu329=