Canonical Allele Identifier: CA2326432172

Gene: CRLF1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596538_18596543delinsAAAAAG , CM000681.2:g.18596538_18596543delinsAAAAAG	GRCh38
NC_000019.9:g.18707348_18707353delinsAAAAAG , CM000681.1:g.18707348_18707353delinsAAAAAG	GRCh37
NC_000019.8:g.18568348_18568353delinsAAAAAG	NCBI36
NG_013370.1:g.15308_15313delinsCTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+79_1024+84delinsCTTTTT	ENSP00000506849.1:n.1024+79_1024+84delinsCTTTTT
ENST00000392386.8:c.1024+79_1024+84delinsCTTTTT MANE Select	ENSP00000376188.2:n.1024+79_1024+84delinsCTTTTT
ENST00000392386.7:c.1024+79_1024+84delinsCTTTTT	ENSP00000376188.2:n.1024+79_1024+84delinsCTTTTT
ENST00000597131.1:c.447+121_447+126delinsCTTTTT
NM_004750.4:c.1024+79_1024+84delinsCTTTTT	NP_004741.1:n.1024+79_1024+84delinsCTTTTT
XM_011528422.1:c.958+79_958+84delinsCTTTTT	XP_011526724.1:n.958+79_958+84delinsCTTTTT
XM_011528423.1:c.1024+79_1024+84delinsCTTTTT	XP_011526725.1:n.1024+79_1024+84delinsCTTTTT
XM_011528424.1:c.958+79_958+84delinsCTTTTT	XP_011526726.1:n.958+79_958+84delinsCTTTTT
XM_011528422.2:c.958+79_958+84delinsCTTTTT	XP_011526724.1:n.958+79_958+84delinsCTTTTT
XM_011528423.2:c.1024+79_1024+84delinsCTTTTT	XP_011526725.1:n.1024+79_1024+84delinsCTTTTT
XM_011528424.3:c.958+79_958+84delinsCTTTTT	XP_011526726.1:n.958+79_958+84delinsCTTTTT
NM_004750.5:c.1024+79_1024+84delinsCTTTTT MANE Select	NP_004741.1:n.1024+79_1024+84delinsCTTTTT