Canonical Allele Identifier: CA675841001

Gene:

Linked Data

• dbSNP Id: rs1169800575
• gnomAD v3: 11-34812279-TCTA-T
• gnomAD v4: 11-34812279-TCTA-T
• MyVariant Identifiers: chr11:g.34833827_34833829del (hg19) ; chr11:g.34812280_34812282del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812281_34812283del , CM000673.2:g.34812281_34812283del	GRCh38
NC_000011.9:g.34833828_34833830del , CM000673.1:g.34833828_34833830del	GRCh37
NC_000011.8:g.34790404_34790406del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57674_579+57676del
XR_931188.1:n.693+57674_693+57676del
XR_931189.1:n.854+57674_854+57676del
XR_931190.1:n.639+57674_639+57676del
XR_931191.1:n.689+57674_689+57676del
XR_001748174.1:n.855+57674_855+57676del
XR_001748176.1:n.1016+57674_1016+57676del
XR_002957246.1:n.639+57674_639+57676del