Canonical Allele Identifier: CA2326433634

Gene: CRLF1

Linked Data

• dbSNP Id: rs1976186903

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599292_18599293del , CM000681.2:g.18599292_18599293del	GRCh38
NC_000019.9:g.18710102_18710103del , CM000681.1:g.18710102_18710103del	GRCh37
NC_000019.8:g.18571102_18571103del	NCBI36
NG_013370.1:g.12561_12562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.397+275_397+276del	ENSP00000506849.1:n.397+275_397+276del
ENST00000392386.8:c.397+275_397+276del MANE Select	ENSP00000376188.2:n.397+275_397+276del
ENST00000392386.7:c.397+275_397+276del	ENSP00000376188.2:n.397+275_397+276del
NM_004750.4:c.397+275_397+276del	NP_004741.1:n.397+275_397+276del
XM_011528422.1:c.331+275_331+276del	XP_011526724.1:n.331+275_331+276del
XM_011528423.1:c.397+275_397+276del	XP_011526725.1:n.397+275_397+276del
XM_011528424.1:c.331+275_331+276del	XP_011526726.1:n.331+275_331+276del
XM_011528422.2:c.331+275_331+276del	XP_011526724.1:n.331+275_331+276del
XM_011528423.2:c.397+275_397+276del	XP_011526725.1:n.397+275_397+276del
XM_011528424.3:c.331+275_331+276del	XP_011526726.1:n.331+275_331+276del
NM_004750.5:c.397+275_397+276del MANE Select	NP_004741.1:n.397+275_397+276del