Canonical Allele Identifier: CA506044665

Gene: CRLF1

Linked Data

• MyVariant Identifiers: chr19:g.18710527_18710528insGGCGCCCGTTGAGGGTCCAGTAGA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599721_18599744dup , CM000681.2:g.18599721_18599744dup	GRCh38
NC_000019.9:g.18710531_18710554dup , CM000681.1:g.18710531_18710554dup	GRCh37
NC_000019.8:g.18571531_18571554dup	NCBI36
NG_013370.1:g.12110_12133dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.221_244dup	ENSP00000506849.1:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg
ENST00000392386.8:c.221_244dup MANE Select	ENSP00000376188.2:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg
ENST00000392386.7:c.221_244dup	ENSP00000376188.2:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg
ENST00000593286.1:n.473_496dup
NM_004750.4:c.221_244dup	NP_004741.1:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg
XM_011528422.1:c.155_178dup	XP_011526724.1:p.Arg59_Arg60insLeuTyrTrpThrLeuAsnGlyArg
XM_011528423.1:c.221_244dup	XP_011526725.1:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg
XM_011528424.1:c.155_178dup	XP_011526726.1:p.Arg59_Arg60insLeuTyrTrpThrLeuAsnGlyArg
XM_011528422.2:c.155_178dup	XP_011526724.1:p.Arg59_Arg60insLeuTyrTrpThrLeuAsnGlyArg
XM_011528423.2:c.221_244dup	XP_011526725.1:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg
XM_011528424.3:c.155_178dup	XP_011526726.1:p.Arg59_Arg60insLeuTyrTrpThrLeuAsnGlyArg
NM_004750.5:c.221_244dup MANE Select	NP_004741.1:p.Arg81_Arg82insLeuTyrTrpThrLeuAsnGlyArg