Canonical Allele Identifier: CA2583603033

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596555-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596556_18596557del , CM000681.2:g.18596556_18596557del	GRCh38
NC_000019.9:g.18707366_18707367del , CM000681.1:g.18707366_18707367del	GRCh37
NC_000019.8:g.18568366_18568367del	NCBI36
NG_013370.1:g.15294_15295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+65_1024+66del	ENSP00000506849.1:n.1024+65_1024+66del
ENST00000392386.8:c.1024+65_1024+66del MANE Select	ENSP00000376188.2:n.1024+65_1024+66del
ENST00000392386.7:c.1024+65_1024+66del	ENSP00000376188.2:n.1024+65_1024+66del
ENST00000597131.1:c.447+107_447+108del
NM_004750.4:c.1024+65_1024+66del	NP_004741.1:n.1024+65_1024+66del
XM_011528422.1:c.958+65_958+66del	XP_011526724.1:n.958+65_958+66del
XM_011528423.1:c.1024+65_1024+66del	XP_011526725.1:n.1024+65_1024+66del
XM_011528424.1:c.958+65_958+66del	XP_011526726.1:n.958+65_958+66del
XM_011528422.2:c.958+65_958+66del	XP_011526724.1:n.958+65_958+66del
XM_011528423.2:c.1024+65_1024+66del	XP_011526725.1:n.1024+65_1024+66del
XM_011528424.3:c.958+65_958+66del	XP_011526726.1:n.958+65_958+66del
NM_004750.5:c.1024+65_1024+66del MANE Select	NP_004741.1:n.1024+65_1024+66del