Canonical Allele Identifier: CA915946613

Gene: STRC

Linked Data

• ClinVar Variation Id: 692158
• ClinVar RCV Id: RCV000853502

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601396_43609335del , CM000677.2:g.43601396_43609335del	GRCh38
NC_000015.9:g.43893594_43901533del , CM000677.1:g.43893594_43901533del	GRCh37
NC_000015.8:g.41680886_41688825del	NCBI36
NG_011636.1:g.14467_22406del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.3499_4701+1del
ENST00000428650.5:c.*531_*1734+1del
ENST00000440125.5:c.*1291_*2493+1del
ENST00000448437.6:n.1370_1821+1del
ENST00000450892.6:c.3499_4701+1del
ENST00000471703.5:n.1282_2655+1del
ENST00000485556.5:n.2490_3556+1del
ENST00000541030.5:c.1180_2382+1del
NM_153700.2:c.3499_4701+1del
XM_011521277.1:c.3988_5190+1del
XM_011521278.1:c.3604_4806+1del
XM_011521279.1:c.3604_4806+1del