Canonical Allele Identifier: CA2583603006

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596532-G-GAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596540_18596542dup , CM000681.2:g.18596540_18596542dup	GRCh38
NC_000019.9:g.18707350_18707352dup , CM000681.1:g.18707350_18707352dup	GRCh37
NC_000019.8:g.18568350_18568352dup	NCBI36
NG_013370.1:g.15316_15318dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+87_1024+89dup	ENSP00000506849.1:n.1024+87_1024+89dup
ENST00000392386.8:c.1024+87_1024+89dup MANE Select	ENSP00000376188.2:n.1024+87_1024+89dup
ENST00000392386.7:c.1024+87_1024+89dup	ENSP00000376188.2:n.1024+87_1024+89dup
ENST00000597131.1:c.447+129_447+131dup
NM_004750.4:c.1024+87_1024+89dup	NP_004741.1:n.1024+87_1024+89dup
XM_011528422.1:c.958+87_958+89dup	XP_011526724.1:n.958+87_958+89dup
XM_011528423.1:c.1024+87_1024+89dup	XP_011526725.1:n.1024+87_1024+89dup
XM_011528424.1:c.958+87_958+89dup	XP_011526726.1:n.958+87_958+89dup
XM_011528422.2:c.958+87_958+89dup	XP_011526724.1:n.958+87_958+89dup
XM_011528423.2:c.1024+87_1024+89dup	XP_011526725.1:n.1024+87_1024+89dup
XM_011528424.3:c.958+87_958+89dup	XP_011526726.1:n.958+87_958+89dup
NM_004750.5:c.1024+87_1024+89dup MANE Select	NP_004741.1:n.1024+87_1024+89dup