Canonical Allele Identifier: CA404850892

Gene: CRLF1

Linked Data

• MyVariant Identifiers: chr19:g.18707750T>G (hg19) ; chr19:g.18596940T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596940T>G , CM000681.2:g.18596940T>G	GRCh38
NC_000019.9:g.18707750T>G , CM000681.1:g.18707750T>G	GRCh37
NC_000019.8:g.18568750T>G	NCBI36
NG_013370.1:g.14911A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.807A>C	ENSP00000506849.1:p.Gln269His
ENST00000392386.8:c.807A>C MANE Select	ENSP00000376188.2:p.Gln269His
ENST00000392386.7:c.807A>C	ENSP00000376188.2:p.Gln269His
ENST00000597131.1:c.272A>C
NM_004750.4:c.807A>C	NP_004741.1:p.Gln269His
XM_011528422.1:c.741A>C	XP_011526724.1:p.Gln247His
XM_011528423.1:c.807A>C	XP_011526725.1:p.Gln269His
XM_011528424.1:c.741A>C	XP_011526726.1:p.Gln247His
XM_011528422.2:c.741A>C	XP_011526724.1:p.Gln247His
XM_011528423.2:c.807A>C	XP_011526725.1:p.Gln269His
XM_011528424.3:c.741A>C	XP_011526726.1:p.Gln247His
NM_004750.5:c.807A>C MANE Select	NP_004741.1:p.Gln269His