Canonical Allele Identifier: CA9314065

Gene: CRLF1

Linked Data

• dbSNP Id: rs540101061
• ExAC: 19:18707621 CAGAGT / C
• gnomAD v2: 19-18707621-CAGAGT-C
• gnomAD v3: 19-18596811-CAGAGT-C
• gnomAD v4: 19-18596811-CAGAGT-C
• MyVariant Identifiers: chr19:g.18707622_18707626del (hg19) ; chr19:g.18596812_18596816del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596816_18596820del , CM000681.2:g.18596816_18596820del	GRCh38
NC_000019.9:g.18707626_18707630del , CM000681.1:g.18707626_18707630del	GRCh37
NC_000019.8:g.18568626_18568630del	NCBI36
NG_013370.1:g.15035_15039del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684169.1:c.856-26_856-22del	ENSP00000506849.1:n.856-26_856-22del
ENST00000392386.8:c.856-26_856-22del MANE Select	ENSP00000376188.2:n.856-26_856-22del
ENST00000392386.7:c.856-26_856-22del	ENSP00000376188.2:n.856-26_856-22del
ENST00000597131.1:c.321-26_321-22del
NM_004750.4:c.856-26_856-22del	NP_004741.1:n.856-26_856-22del
XM_011528422.1:c.790-26_790-22del	XP_011526724.1:n.790-26_790-22del
XM_011528423.1:c.856-26_856-22del	XP_011526725.1:n.856-26_856-22del
XM_011528424.1:c.790-26_790-22del	XP_011526726.1:n.790-26_790-22del
XM_011528422.2:c.790-26_790-22del	XP_011526724.1:n.790-26_790-22del
XM_011528423.2:c.856-26_856-22del	XP_011526725.1:n.856-26_856-22del
XM_011528424.3:c.790-26_790-22del	XP_011526726.1:n.790-26_790-22del
NM_004750.5:c.856-26_856-22del MANE Select	NP_004741.1:n.856-26_856-22del