Canonical Allele Identifier: CA506116384

Gene: CRLF1

Linked Data

• ClinVar Variation Id: 735827
• ClinVar RCV Id: RCV000911419
• dbSNP Id: rs1600651281
• MyVariant Identifiers: chr19:g.18707771G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596961G>A , CM000681.2:g.18596961G>A	GRCh38
NC_000019.9:g.18707771G>A , CM000681.1:g.18707771G>A	GRCh37
NC_000019.8:g.18568771G>A	NCBI36
NG_013370.1:g.14890C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.786C>T	ENSP00000506849.1:p.Ala262=
ENST00000392386.8:c.786C>T MANE Select	ENSP00000376188.2:p.Ala262=
ENST00000392386.7:c.786C>T	ENSP00000376188.2:p.Ala262=
ENST00000597131.1:c.251C>T
NM_004750.4:c.786C>T	NP_004741.1:p.Ala262=
XM_011528422.1:c.720C>T	XP_011526724.1:p.Ala240=
XM_011528423.1:c.786C>T	XP_011526725.1:p.Ala262=
XM_011528424.1:c.720C>T	XP_011526726.1:p.Ala240=
XM_011528422.2:c.720C>T	XP_011526724.1:p.Ala240=
XM_011528423.2:c.786C>T	XP_011526725.1:p.Ala262=
XM_011528424.3:c.720C>T	XP_011526726.1:p.Ala240=
NM_004750.5:c.786C>T MANE Select	NP_004741.1:p.Ala262=