Canonical Allele Identifier: CA2583603005

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596531-AGAAAAAAAAAAGAAAAGAAAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596532_18596553del , CM000681.2:g.18596532_18596553del	GRCh38
NC_000019.9:g.18707342_18707363del , CM000681.1:g.18707342_18707363del	GRCh37
NC_000019.8:g.18568342_18568363del	NCBI36
NG_013370.1:g.15298_15319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+69_1024+90del	ENSP00000506849.1:n.1024+69_1024+90del
ENST00000392386.8:c.1024+69_1024+90del MANE Select	ENSP00000376188.2:n.1024+69_1024+90del
ENST00000392386.7:c.1024+69_1024+90del	ENSP00000376188.2:n.1024+69_1024+90del
ENST00000597131.1:c.447+111_447+132del
NM_004750.4:c.1024+69_1024+90del	NP_004741.1:n.1024+69_1024+90del
XM_011528422.1:c.958+69_958+90del	XP_011526724.1:n.958+69_958+90del
XM_011528423.1:c.1024+69_1024+90del	XP_011526725.1:n.1024+69_1024+90del
XM_011528424.1:c.958+69_958+90del	XP_011526726.1:n.958+69_958+90del
XM_011528422.2:c.958+69_958+90del	XP_011526724.1:n.958+69_958+90del
XM_011528423.2:c.1024+69_1024+90del	XP_011526725.1:n.1024+69_1024+90del
XM_011528424.3:c.958+69_958+90del	XP_011526726.1:n.958+69_958+90del
NM_004750.5:c.1024+69_1024+90del MANE Select	NP_004741.1:n.1024+69_1024+90del