Canonical Allele Identifier: CA2396362234

Gene: SCARF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425149_20425157delinsGCTAAGCGC , CM000684.2:g.20425149_20425157delinsGCTAAGCGC	GRCh38
NC_000022.10:g.20779439_20779447delinsGCTAAGCGC , CM000684.1:g.20779439_20779447delinsGCTAAGCGC	GRCh37
NC_000022.9:g.19109439_19109447delinsGCTAAGCGC	NCBI36
NG_031868.2:g.17703_17711delinsGCGCTTAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.*218_*226delinsGCGCTTAGC MANE Select	ENSP00000477564.2:n.*218_*226delinsGCGCTTAGC
ENST00000615031.4:c.*218_*226delinsGCGCTTAGC	ENSP00000479389.1:n.*218_*226delinsGCGCTTAGC
ENST00000622235.4:c.*218_*226delinsGCGCTTAGC	ENSP00000477564.1:n.*218_*226delinsGCGCTTAGC
ENST00000623402.1:c.*218_*226delinsGCGCTTAGC	ENSP00000485276.1:n.*218_*226delinsGCGCTTAGC
NM_153334.6:c.*218_*226delinsGCGCTTAGC	NP_699165.3:n.*218_*226delinsGCGCTTAGC
NM_182895.4:c.*218_*226delinsGCGCTTAGC	NP_878315.2:n.*218_*226delinsGCGCTTAGC
NM_153334.7:c.*218_*226delinsGCGCTTAGC	NP_699165.3:n.*218_*226delinsGCGCTTAGC
NM_182895.5:c.*218_*226delinsGCGCTTAGC MANE Select	NP_878315.2:n.*218_*226delinsGCGCTTAGC