Canonical Allele Identifier: CA2583603020

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596542-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596542_18596543insT , CM000681.2:g.18596542_18596543insT	GRCh38
NC_000019.9:g.18707352_18707353insT , CM000681.1:g.18707352_18707353insT	GRCh37
NC_000019.8:g.18568352_18568353insT	NCBI36
NG_013370.1:g.15308_15309insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+79_1024+80insA	ENSP00000506849.1:n.1024+79_1024+80insA
ENST00000392386.8:c.1024+79_1024+80insA MANE Select	ENSP00000376188.2:n.1024+79_1024+80insA
ENST00000392386.7:c.1024+79_1024+80insA	ENSP00000376188.2:n.1024+79_1024+80insA
ENST00000597131.1:c.447+121_447+122insA
NM_004750.4:c.1024+79_1024+80insA	NP_004741.1:n.1024+79_1024+80insA
XM_011528422.1:c.958+79_958+80insA	XP_011526724.1:n.958+79_958+80insA
XM_011528423.1:c.1024+79_1024+80insA	XP_011526725.1:n.1024+79_1024+80insA
XM_011528424.1:c.958+79_958+80insA	XP_011526726.1:n.958+79_958+80insA
XM_011528422.2:c.958+79_958+80insA	XP_011526724.1:n.958+79_958+80insA
XM_011528423.2:c.1024+79_1024+80insA	XP_011526725.1:n.1024+79_1024+80insA
XM_011528424.3:c.958+79_958+80insA	XP_011526726.1:n.958+79_958+80insA
NM_004750.5:c.1024+79_1024+80insA MANE Select	NP_004741.1:n.1024+79_1024+80insA