Canonical Allele Identifier: CA2583603022

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596544-AAAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596548_18596551del , CM000681.2:g.18596548_18596551del	GRCh38
NC_000019.9:g.18707358_18707361del , CM000681.1:g.18707358_18707361del	GRCh37
NC_000019.8:g.18568358_18568361del	NCBI36
NG_013370.1:g.15303_15306del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+74_1024+77del	ENSP00000506849.1:n.1024+74_1024+77del
ENST00000392386.8:c.1024+74_1024+77del MANE Select	ENSP00000376188.2:n.1024+74_1024+77del
ENST00000392386.7:c.1024+74_1024+77del	ENSP00000376188.2:n.1024+74_1024+77del
ENST00000597131.1:c.447+116_447+119del
NM_004750.4:c.1024+74_1024+77del	NP_004741.1:n.1024+74_1024+77del
XM_011528422.1:c.958+74_958+77del	XP_011526724.1:n.958+74_958+77del
XM_011528423.1:c.1024+74_1024+77del	XP_011526725.1:n.1024+74_1024+77del
XM_011528424.1:c.958+74_958+77del	XP_011526726.1:n.958+74_958+77del
XM_011528422.2:c.958+74_958+77del	XP_011526724.1:n.958+74_958+77del
XM_011528423.2:c.1024+74_1024+77del	XP_011526725.1:n.1024+74_1024+77del
XM_011528424.3:c.958+74_958+77del	XP_011526726.1:n.958+74_958+77del
NM_004750.5:c.1024+74_1024+77del MANE Select	NP_004741.1:n.1024+74_1024+77del