Canonical Allele Identifier: CA404851071

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18597031-G-C
• MyVariant Identifiers: chr19:g.18707841G>C (hg19) ; chr19:g.18597031G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18597031G>C , CM000681.2:g.18597031G>C	GRCh38
NC_000019.9:g.18707841G>C , CM000681.1:g.18707841G>C	GRCh37
NC_000019.8:g.18568841G>C	NCBI36
NG_013370.1:g.14820C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.716C>G	ENSP00000506849.1:p.Pro239Arg
ENST00000392386.8:c.716C>G MANE Select	ENSP00000376188.2:p.Pro239Arg
ENST00000392386.7:c.716C>G	ENSP00000376188.2:p.Pro239Arg
ENST00000597131.1:c.181C>G
NM_004750.4:c.716C>G	NP_004741.1:p.Pro239Arg
XM_011528422.1:c.650C>G	XP_011526724.1:p.Pro217Arg
XM_011528423.1:c.716C>G	XP_011526725.1:p.Pro239Arg
XM_011528424.1:c.650C>G	XP_011526726.1:p.Pro217Arg
XM_011528422.2:c.650C>G	XP_011526724.1:p.Pro217Arg
XM_011528423.2:c.716C>G	XP_011526725.1:p.Pro239Arg
XM_011528424.3:c.650C>G	XP_011526726.1:p.Pro217Arg
NM_004750.5:c.716C>G MANE Select	NP_004741.1:p.Pro239Arg