Canonical Allele Identifier: CA2573054010

Gene: STRC

Linked Data

• ClinVar Variation Id: 1185095
• ClinVar RCV Id: RCV001822917

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599672_43609276del , CM000677.2:g.43599672_43609276del	GRCh38
NC_000015.9:g.43891870_43901474del , CM000677.1:g.43891870_43901474del	GRCh37
NC_000015.8:g.41679162_41688766del	NCBI36
NG_011636.1:g.14525_24129del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.3557_5328del
ENST00000428650.5:c.*589_*2361del
ENST00000440125.5:c.*1349_*3120del
ENST00000448437.6:n.1428_2448del
ENST00000450892.6:c.3557_5328del
ENST00000471703.5:n.1340_3282del
ENST00000485556.5:n.2548_4183del
ENST00000541030.5:c.1238_3009del
NM_153700.2:c.3557_5328del
XM_011521277.1:c.4046_5817del
XM_011521278.1:c.3662_5433del
XM_011521279.1:c.3662_5433del