Canonical Allele Identifier: CA2583602966

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596493-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596497_18596498del , CM000681.2:g.18596497_18596498del	GRCh38
NC_000019.9:g.18707307_18707308del , CM000681.1:g.18707307_18707308del	GRCh37
NC_000019.8:g.18568307_18568308del	NCBI36
NG_013370.1:g.15356_15357del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+127_1024+128del	ENSP00000506849.1:n.1024+127_1024+128del
ENST00000392386.8:c.1024+127_1024+128del MANE Select	ENSP00000376188.2:n.1024+127_1024+128del
ENST00000392386.7:c.1024+127_1024+128del	ENSP00000376188.2:n.1024+127_1024+128del
ENST00000597131.1:c.447+169_447+170del
NM_004750.4:c.1024+127_1024+128del	NP_004741.1:n.1024+127_1024+128del
XM_011528422.1:c.958+127_958+128del	XP_011526724.1:n.958+127_958+128del
XM_011528423.1:c.1024+127_1024+128del	XP_011526725.1:n.1024+127_1024+128del
XM_011528424.1:c.958+127_958+128del	XP_011526726.1:n.958+127_958+128del
XM_011528422.2:c.958+127_958+128del	XP_011526724.1:n.958+127_958+128del
XM_011528423.2:c.1024+127_1024+128del	XP_011526725.1:n.1024+127_1024+128del
XM_011528424.3:c.958+127_958+128del	XP_011526726.1:n.958+127_958+128del
NM_004750.5:c.1024+127_1024+128del MANE Select	NP_004741.1:n.1024+127_1024+128del