Canonical Allele Identifier: CA632364896

Gene: CRLF1

Linked Data

• dbSNP Id: rs1280850734
• gnomAD v2: 19-18707348-AAAAAG-A
• gnomAD v3: 19-18596538-AAAAAG-A
• gnomAD v4: 19-18596538-AAAAAG-A
• MyVariant Identifiers: chr19:g.18707349_18707353del (hg19) ; chr19:g.18596539_18596543del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596548_18596552del , CM000681.2:g.18596548_18596552del	GRCh38
NC_000019.9:g.18707358_18707362del , CM000681.1:g.18707358_18707362del	GRCh37
NC_000019.8:g.18568358_18568362del	NCBI36
NG_013370.1:g.15308_15312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+79_1024+83del	ENSP00000506849.1:n.1024+79_1024+83del
ENST00000392386.8:c.1024+79_1024+83del MANE Select	ENSP00000376188.2:n.1024+79_1024+83del
ENST00000392386.7:c.1024+79_1024+83del	ENSP00000376188.2:n.1024+79_1024+83del
ENST00000597131.1:c.447+121_447+125del
NM_004750.4:c.1024+79_1024+83del	NP_004741.1:n.1024+79_1024+83del
XM_011528422.1:c.958+79_958+83del	XP_011526724.1:n.958+79_958+83del
XM_011528423.1:c.1024+79_1024+83del	XP_011526725.1:n.1024+79_1024+83del
XM_011528424.1:c.958+79_958+83del	XP_011526726.1:n.958+79_958+83del
XM_011528422.2:c.958+79_958+83del	XP_011526724.1:n.958+79_958+83del
XM_011528423.2:c.1024+79_1024+83del	XP_011526725.1:n.1024+79_1024+83del
XM_011528424.3:c.958+79_958+83del	XP_011526726.1:n.958+79_958+83del
NM_004750.5:c.1024+79_1024+83del MANE Select	NP_004741.1:n.1024+79_1024+83del