Canonical Allele Identifier: CA029854

Gene: CRLF1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.[18594338A>C;18599720C>T] , CM000681.2:g.[18594338A>C;18599720C>T]	GRCh38
NC_000019.9:g.[18705148A>C;18710530C>T] , CM000681.1:g.[18705148A>C;18710530C>T]	GRCh37
NC_000019.8:g.[18566148A>C;18571530C>T]	NCBI36
NG_013370.1:g.[12131G>A;17513T>G]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.[242G>A;1121T>G]	ENSP00000506849.1:p.[Arg81His;Leu374Arg]
ENST00000392386.8:c.[242G>A;1121T>G] MANE Select	ENSP00000376188.2:p.[Arg81His;Leu374Arg]
ENST00000392386.7:c.[242G>A;1121T>G]	ENSP00000376188.2:p.[Arg81His;Leu374Arg]
NM_004750.4:c.[242G>A;1121T>G]	NP_004741.1:p.[Arg81His;Leu374Arg]
XM_011528422.1:c.[176G>A;1055T>G]	XP_011526724.1:p.[Arg59His;Leu352Arg]
XM_011528423.1:c.[242G>A;1121T>G]	XP_011526725.1:p.[Arg81His;Leu374Arg]
XM_011528424.1:c.[176G>A;1055T>G]	XP_011526726.1:p.[Arg59His;Leu352Arg]
XM_011528422.2:c.[176G>A;1055T>G]	XP_011526724.1:p.[Arg59His;Leu352Arg]
XM_011528423.2:c.[242G>A;1121T>G]	XP_011526725.1:p.[Arg81His;Leu374Arg]
XM_011528424.3:c.[176G>A;1055T>G]	XP_011526726.1:p.[Arg59His;Leu352Arg]
NM_004750.5:c.[242G>A;1121T>G] MANE Select	NP_004741.1:p.[Arg81His;Leu374Arg]