Canonical Allele Identifier: CA2583603782

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18599763-G-GCGGCGAAGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599763_18599764insCGGCGAAGGCC , CM000681.2:g.18599763_18599764insCGGCGAAGGCC	GRCh38
NC_000019.9:g.18710573_18710574insCGGCGAAGGCC , CM000681.1:g.18710573_18710574insCGGCGAAGGCC	GRCh37
NC_000019.8:g.18571573_18571574insCGGCGAAGGCC	NCBI36
NG_013370.1:g.12087_12088insGGCCTTCGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.198_199insGGCCTTCGCCG	ENSP00000506849.1:p.Pro67GlyfsTer?
ENST00000392386.8:c.198_199insGGCCTTCGCCG MANE Select	ENSP00000376188.2:p.Pro67GlyfsTer?
ENST00000392386.7:c.198_199insGGCCTTCGCCG	ENSP00000376188.2:p.Pro67GlyfsTer?
ENST00000593286.1:n.450_451insGGCCTTCGCCG
NM_004750.4:c.198_199insGGCCTTCGCCG	NP_004741.1:p.Pro67GlyfsTer?
XM_011528422.1:c.132_133insGGCCTTCGCCG	XP_011526724.1:p.Pro45GlyfsTer?
XM_011528423.1:c.198_199insGGCCTTCGCCG	XP_011526725.1:p.Pro67GlyfsTer?
XM_011528424.1:c.132_133insGGCCTTCGCCG	XP_011526726.1:p.Pro45GlyfsTer?
XM_011528422.2:c.132_133insGGCCTTCGCCG	XP_011526724.1:p.Pro45GlyfsTer?
XM_011528423.2:c.198_199insGGCCTTCGCCG	XP_011526725.1:p.Pro67GlyfsTer?
XM_011528424.3:c.132_133insGGCCTTCGCCG	XP_011526726.1:p.Pro45GlyfsTer?
NM_004750.5:c.198_199insGGCCTTCGCCG MANE Select	NP_004741.1:p.Pro67GlyfsTer?