Canonical Allele Identifier: CA704066459

Gene: OSGEP

Linked Data

• dbSNP Id: rs1354246013
• MyVariant Identifiers: chr14:g.20923070_20923071insGTTTTCCTA (hg19) ; chr14:g.20454911_20454912insGTTTTCCTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20454911_20454912insGTTTTCCTA , CM000676.2:g.20454911_20454912insGTTTTCCTA	GRCh38
NC_000014.8:g.20923070_20923071insGTTTTCCTA , CM000676.1:g.20923070_20923071insGTTTTCCTA	GRCh37
NC_000014.7:g.19992910_19992911insGTTTTCCTA	NCBI36
NG_008718.1:g.4781_4782insGTTTTCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206542.8:c.-229_-228insTAGGAAAAC	ENSP00000206542.4:n.-229_-228insTAGGAAAAC
ENST00000556252.1:n.142_143insTAGGAAAAC
ENST00000556439.1:n.178_179insTAGGAAAAC
NM_017807.3:c.-229_-228insTAGGAAAAC	NP_060277.1:n.-229_-228insTAGGAAAAC
XM_011536930.1:c.-290_-289insTAGGAAAAC	XP_011535232.1:n.-290_-289insTAGGAAAAC