Canonical Allele Identifier: CA2326432324

Gene: CRLF1

Linked Data

• dbSNP Id: rs1976141451
• gnomAD v4: 19-18596819-AGGGCGGGGCCTAGCAGGAGCGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596831_18596852del , CM000681.2:g.18596831_18596852del	GRCh38
NC_000019.9:g.18707641_18707662del , CM000681.1:g.18707641_18707662del	GRCh37
NC_000019.8:g.18568641_18568662del	NCBI36
NG_013370.1:g.15010_15031del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684169.1:c.856-51_856-30del	ENSP00000506849.1:n.856-51_856-30del
ENST00000392386.8:c.856-51_856-30del MANE Select	ENSP00000376188.2:n.856-51_856-30del
ENST00000392386.7:c.856-51_856-30del	ENSP00000376188.2:n.856-51_856-30del
ENST00000597131.1:c.321-51_321-30del
NM_004750.4:c.856-51_856-30del	NP_004741.1:n.856-51_856-30del
XM_011528422.1:c.790-51_790-30del	XP_011526724.1:n.790-51_790-30del
XM_011528423.1:c.856-51_856-30del	XP_011526725.1:n.856-51_856-30del
XM_011528424.1:c.790-51_790-30del	XP_011526726.1:n.790-51_790-30del
XM_011528422.2:c.790-51_790-30del	XP_011526724.1:n.790-51_790-30del
XM_011528423.2:c.856-51_856-30del	XP_011526725.1:n.856-51_856-30del
XM_011528424.3:c.790-51_790-30del	XP_011526726.1:n.790-51_790-30del
NM_004750.5:c.856-51_856-30del MANE Select	NP_004741.1:n.856-51_856-30del