Canonical Allele Identifier: CA675841003

Gene:

Linked Data

• dbSNP Id: rs1374289657
• gnomAD v3: 11-34812288-G-GA
• gnomAD v4: 11-34812288-G-GA
• MyVariant Identifiers: chr11:g.34833835_34833836insA (hg19) ; chr11:g.34812288_34812289insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812294dup , CM000673.2:g.34812294dup	GRCh38
NC_000011.9:g.34833841dup , CM000673.1:g.34833841dup	GRCh37
NC_000011.8:g.34790417dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57687dup
XR_931188.1:n.693+57687dup
XR_931189.1:n.854+57687dup
XR_931190.1:n.639+57687dup
XR_931191.1:n.689+57687dup
XR_001748174.1:n.855+57687dup
XR_001748176.1:n.1016+57687dup
XR_002957246.1:n.639+57687dup