Canonical Allele Identifier: CA675841052

Gene:

Linked Data

• dbSNP Id: rs1383330413
• MyVariant Identifiers: chr11:g.34834055_34834067del (hg19) ; chr11:g.34812508_34812520del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812509_34812521del , CM000673.2:g.34812509_34812521del	GRCh38
NC_000011.9:g.34834056_34834068del , CM000673.1:g.34834056_34834068del	GRCh37
NC_000011.8:g.34790632_34790644del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57902_579+57914del
XR_931188.1:n.693+57902_693+57914del
XR_931189.1:n.854+57902_854+57914del
XR_931190.1:n.639+57902_639+57914del
XR_931191.1:n.689+57902_689+57914del
XR_001748174.1:n.855+57902_855+57914del
XR_001748176.1:n.1016+57902_1016+57914del
XR_002957246.1:n.639+57902_639+57914del