Canonical Allele Identifier: CA270010418

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43605623del , CM000677.2:g.43605623del	GRCh38
NC_000015.9:g.43897821del , CM000677.1:g.43897821del	GRCh37
NC_000015.8:g.41685113del	NCBI36
NG_011636.1:g.18189del

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.3795-213del MANE Select	NP_714544.1:n.3795-213del
ENST00000450892.7:c.3795-213del MANE Select	ENSP00000401513.2:n.3795-213del
ENST00000428650.5:c.*827-213del	ENSP00000415991.1:n.*827-213del
ENST00000440125.5:c.*1587-213del	ENSP00000394866.1:n.*1587-213del
ENST00000448437.6:n.1665+2251del
ENST00000450892.6:c.3795-213del	ENSP00000401513.2:n.3795-213del
ENST00000455136.5:c.826-213del
ENST00000471703.5:n.1578-213del
ENST00000485556.5:n.2786-766del
ENST00000541030.5:c.1476-213del	ENSP00000440413.1:n.1476-213del
XM_011521277.1:c.4284-213del	XP_011519579.1:n.4284-213del
XM_011521278.1:c.3900-213del	XP_011519580.1:n.3900-213del
XM_011521279.1:c.3900-213del	XP_011519581.1:n.3900-213del