Canonical Allele Identifier: CA404852308

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18599825-T-C
• MyVariant Identifiers: chr19:g.18710635T>C (hg19) ; chr19:g.18599825T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599825T>C , CM000681.2:g.18599825T>C	GRCh38
NC_000019.9:g.18710635T>C , CM000681.1:g.18710635T>C	GRCh37
NC_000019.8:g.18571635T>C	NCBI36
NG_013370.1:g.12026A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.137A>G	ENSP00000506849.1:p.Gln46Arg
ENST00000392386.8:c.137A>G MANE Select	ENSP00000376188.2:p.Gln46Arg
ENST00000392386.7:c.137A>G	ENSP00000376188.2:p.Gln46Arg
ENST00000593286.1:n.389A>G
NM_004750.4:c.137A>G	NP_004741.1:p.Gln46Arg
XM_011528422.1:c.71A>G	XP_011526724.1:p.Gln24Arg
XM_011528423.1:c.137A>G	XP_011526725.1:p.Gln46Arg
XM_011528424.1:c.71A>G	XP_011526726.1:p.Gln24Arg
XM_011528422.2:c.71A>G	XP_011526724.1:p.Gln24Arg
XM_011528423.2:c.137A>G	XP_011526725.1:p.Gln46Arg
XM_011528424.3:c.71A>G	XP_011526726.1:p.Gln24Arg
NM_004750.5:c.137A>G MANE Select	NP_004741.1:p.Gln46Arg