Canonical Allele Identifier: CA404852244

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18599790-C-T
• MyVariant Identifiers: chr19:g.18710600C>T (hg19) ; chr19:g.18599790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599790C>T , CM000681.2:g.18599790C>T	GRCh38
NC_000019.9:g.18710600C>T , CM000681.1:g.18710600C>T	GRCh37
NC_000019.8:g.18571600C>T	NCBI36
NG_013370.1:g.12061G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.172G>A	ENSP00000506849.1:p.Ala58Thr
ENST00000392386.8:c.172G>A MANE Select	ENSP00000376188.2:p.Ala58Thr
ENST00000392386.7:c.172G>A	ENSP00000376188.2:p.Ala58Thr
ENST00000593286.1:n.424G>A
NM_004750.4:c.172G>A	NP_004741.1:p.Ala58Thr
XM_011528422.1:c.106G>A	XP_011526724.1:p.Ala36Thr
XM_011528423.1:c.172G>A	XP_011526725.1:p.Ala58Thr
XM_011528424.1:c.106G>A	XP_011526726.1:p.Ala36Thr
XM_011528422.2:c.106G>A	XP_011526724.1:p.Ala36Thr
XM_011528423.2:c.172G>A	XP_011526725.1:p.Ala58Thr
XM_011528424.3:c.106G>A	XP_011526726.1:p.Ala36Thr
NM_004750.5:c.172G>A MANE Select	NP_004741.1:p.Ala58Thr