Canonical Allele Identifier: CA404850900

Gene: CRLF1

Linked Data

• MyVariant Identifiers: chr19:g.18707754A>C (hg19) ; chr19:g.18596944A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596944A>C , CM000681.2:g.18596944A>C	GRCh38
NC_000019.9:g.18707754A>C , CM000681.1:g.18707754A>C	GRCh37
NC_000019.8:g.18568754A>C	NCBI36
NG_013370.1:g.14907T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.803T>G	ENSP00000506849.1:p.Phe268Cys
ENST00000392386.8:c.803T>G MANE Select	ENSP00000376188.2:p.Phe268Cys
ENST00000392386.7:c.803T>G	ENSP00000376188.2:p.Phe268Cys
ENST00000597131.1:c.268T>G
NM_004750.4:c.803T>G	NP_004741.1:p.Phe268Cys
XM_011528422.1:c.737T>G	XP_011526724.1:p.Phe246Cys
XM_011528423.1:c.803T>G	XP_011526725.1:p.Phe268Cys
XM_011528424.1:c.737T>G	XP_011526726.1:p.Phe246Cys
XM_011528422.2:c.737T>G	XP_011526724.1:p.Phe246Cys
XM_011528423.2:c.803T>G	XP_011526725.1:p.Phe268Cys
XM_011528424.3:c.737T>G	XP_011526726.1:p.Phe246Cys
NM_004750.5:c.803T>G MANE Select	NP_004741.1:p.Phe268Cys