Canonical Allele Identifier: CA506044100

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18594355-C-T
• MyVariant Identifiers: chr19:g.18705165C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18594355C>T , CM000681.2:g.18594355C>T	GRCh38
NC_000019.9:g.18705165C>T , CM000681.1:g.18705165C>T	GRCh37
NC_000019.8:g.18566165C>T	NCBI36
NG_013370.1:g.17496G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684169.1:c.1104G>A	ENSP00000506849.1:p.Lys368=
ENST00000392386.8:c.1104G>A MANE Select	ENSP00000376188.2:p.Lys368=
ENST00000392386.7:c.1104G>A	ENSP00000376188.2:p.Lys368=
ENST00000594325.1:n.81G>A
NM_004750.4:c.1104G>A	NP_004741.1:p.Lys368=
XM_011528422.1:c.1038G>A	XP_011526724.1:p.Lys346=
XM_011528423.1:c.1104G>A	XP_011526725.1:p.Lys368=
XM_011528424.1:c.1038G>A	XP_011526726.1:p.Lys346=
XM_011528422.2:c.1038G>A	XP_011526724.1:p.Lys346=
XM_011528423.2:c.1104G>A	XP_011526725.1:p.Lys368=
XM_011528424.3:c.1038G>A	XP_011526726.1:p.Lys346=
NM_004750.5:c.1104G>A MANE Select	NP_004741.1:p.Lys368=