Canonical Allele Identifier: CA2583603017

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596541-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596541_18596542insG , CM000681.2:g.18596541_18596542insG	GRCh38
NC_000019.9:g.18707351_18707352insG , CM000681.1:g.18707351_18707352insG	GRCh37
NC_000019.8:g.18568351_18568352insG	NCBI36
NG_013370.1:g.15309_15310insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+80_1024+81insC	ENSP00000506849.1:n.1024+80_1024+81insC
ENST00000392386.8:c.1024+80_1024+81insC MANE Select	ENSP00000376188.2:n.1024+80_1024+81insC
ENST00000392386.7:c.1024+80_1024+81insC	ENSP00000376188.2:n.1024+80_1024+81insC
ENST00000597131.1:c.447+122_447+123insC
NM_004750.4:c.1024+80_1024+81insC	NP_004741.1:n.1024+80_1024+81insC
XM_011528422.1:c.958+80_958+81insC	XP_011526724.1:n.958+80_958+81insC
XM_011528423.1:c.1024+80_1024+81insC	XP_011526725.1:n.1024+80_1024+81insC
XM_011528424.1:c.958+80_958+81insC	XP_011526726.1:n.958+80_958+81insC
XM_011528422.2:c.958+80_958+81insC	XP_011526724.1:n.958+80_958+81insC
XM_011528423.2:c.1024+80_1024+81insC	XP_011526725.1:n.1024+80_1024+81insC
XM_011528424.3:c.958+80_958+81insC	XP_011526726.1:n.958+80_958+81insC
NM_004750.5:c.1024+80_1024+81insC MANE Select	NP_004741.1:n.1024+80_1024+81insC