Canonical Allele Identifier: CA660863687

Gene:

Linked Data

• dbSNP Id: rs1459143895
• MyVariant Identifiers: chr10:g.124217793_124217794del (hg19) ; chr10:g.122458277_122458278del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458277_122458278del , CM000672.2:g.122458277_122458278del	GRCh38
NC_000010.10:g.124217793_124217794del , CM000672.1:g.124217793_124217794del	GRCh37
NC_000010.9:g.124207783_124207784del	NCBI36
NG_011554.1:g.1753_1754del
NG_011725.1:g.8615_8616del

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+217_1827+218del
XR_946383.1:n.1827+217_1827+218del
XR_946384.1:n.1576+217_1576+218del
XR_946385.1:n.1827+217_1827+218del
XR_946382.2:n.1855+217_1855+218del
XR_946383.2:n.1855+217_1855+218del
XR_946384.2:n.1580+217_1580+218del
XR_946385.2:n.1855+217_1855+218del