Canonical Allele Identifier: CA506044049

Gene: CRLF1

Linked Data

• MyVariant Identifiers: chr19:g.18705066G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18594256G>C , CM000681.2:g.18594256G>C	GRCh38
NC_000019.9:g.18705066G>C , CM000681.1:g.18705066G>C	GRCh37
NC_000019.8:g.18566066G>C	NCBI36
NG_013370.1:g.17595C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1203C>G	ENSP00000506849.1:p.Thr401=
ENST00000392386.8:c.1203C>G MANE Select	ENSP00000376188.2:p.Thr401=
ENST00000392386.7:c.1203C>G	ENSP00000376188.2:p.Thr401=
ENST00000594325.1:n.180C>G
NM_004750.4:c.1203C>G	NP_004741.1:p.Thr401=
XM_011528422.1:c.1137C>G	XP_011526724.1:p.Thr379=
XM_011528423.1:c.1203C>G	XP_011526725.1:p.Thr401=
XM_011528424.1:c.1137C>G	XP_011526726.1:p.Thr379=
XM_011528422.2:c.1137C>G	XP_011526724.1:p.Thr379=
XM_011528423.2:c.1203C>G	XP_011526725.1:p.Thr401=
XM_011528424.3:c.1137C>G	XP_011526726.1:p.Thr379=
NM_004750.5:c.1203C>G MANE Select	NP_004741.1:p.Thr401=