Canonical Allele Identifier: CA306262061

Gene: CRLF1

Linked Data

• dbSNP Id: rs948418271
• MyVariant Identifiers: chr19:g.18710190_18710191del (hg19) ; chr19:g.18599380_18599381del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599381_18599382del , CM000681.2:g.18599381_18599382del	GRCh38
NC_000019.9:g.18710191_18710192del , CM000681.1:g.18710191_18710192del	GRCh37
NC_000019.8:g.18571191_18571192del	NCBI36
NG_013370.1:g.12470_12471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.397+184_397+185del	ENSP00000506849.1:n.397+184_397+185del
ENST00000392386.8:c.397+184_397+185del MANE Select	ENSP00000376188.2:n.397+184_397+185del
ENST00000392386.7:c.397+184_397+185del	ENSP00000376188.2:n.397+184_397+185del
NM_004750.4:c.397+184_397+185del	NP_004741.1:n.397+184_397+185del
XM_011528422.1:c.331+184_331+185del	XP_011526724.1:n.331+184_331+185del
XM_011528423.1:c.397+184_397+185del	XP_011526725.1:n.397+184_397+185del
XM_011528424.1:c.331+184_331+185del	XP_011526726.1:n.331+184_331+185del
XM_011528422.2:c.331+184_331+185del	XP_011526724.1:n.331+184_331+185del
XM_011528423.2:c.397+184_397+185del	XP_011526725.1:n.397+184_397+185del
XM_011528424.3:c.331+184_331+185del	XP_011526726.1:n.331+184_331+185del
NM_004750.5:c.397+184_397+185del MANE Select	NP_004741.1:n.397+184_397+185del