Canonical Allele Identifier: CA2583603783

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18599777-A-ACCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599778_18599779insCACC , CM000681.2:g.18599778_18599779insCACC	GRCh38
NC_000019.9:g.18710588_18710589insCACC , CM000681.1:g.18710588_18710589insCACC	GRCh37
NC_000019.8:g.18571588_18571589insCACC	NCBI36
NG_013370.1:g.12073_12074insGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.184_185insGTGG	ENSP00000506849.1:p.Val62GlyfsTer26
ENST00000392386.8:c.184_185insGTGG MANE Select	ENSP00000376188.2:p.Val62GlyfsTer26
ENST00000392386.7:c.184_185insGTGG	ENSP00000376188.2:p.Val62GlyfsTer26
ENST00000593286.1:n.436_437insGTGG
NM_004750.4:c.184_185insGTGG	NP_004741.1:p.Val62GlyfsTer26
XM_011528422.1:c.118_119insGTGG	XP_011526724.1:p.Val40GlyfsTer26
XM_011528423.1:c.184_185insGTGG	XP_011526725.1:p.Val62GlyfsTer26
XM_011528424.1:c.118_119insGTGG	XP_011526726.1:p.Val40GlyfsTer26
XM_011528422.2:c.118_119insGTGG	XP_011526724.1:p.Val40GlyfsTer26
XM_011528423.2:c.184_185insGTGG	XP_011526725.1:p.Val62GlyfsTer26
XM_011528424.3:c.118_119insGTGG	XP_011526726.1:p.Val40GlyfsTer26
NM_004750.5:c.184_185insGTGG MANE Select	NP_004741.1:p.Val62GlyfsTer26