Canonical Allele Identifier: CA675837327

Gene:

Linked Data

• dbSNP Id: rs1271680063
• MyVariant Identifiers: chr11:g.34780852_34780856del (hg19) ; chr11:g.34759305_34759309del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34759309_34759313del , CM000673.2:g.34759309_34759313del	GRCh38
NC_000011.9:g.34780856_34780860del , CM000673.1:g.34780856_34780860del	GRCh37
NC_000011.8:g.34737432_34737436del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+4702_579+4706del
XR_931188.1:n.693+4702_693+4706del
XR_931189.1:n.854+4702_854+4706del
XR_931190.1:n.639+4702_639+4706del
XR_931191.1:n.689+4702_689+4706del
XR_001748174.1:n.855+4702_855+4706del
XR_001748176.1:n.1016+4702_1016+4706del
XR_002957246.1:n.639+4702_639+4706del