Canonical Allele Identifier: CA784842249

Gene:

Linked Data

• dbSNP Id: rs1467363651
• MyVariant Identifiers: chr4:g.106463647_106463654del (hg19) ; chr4:g.105542490_105542497del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542493_105542500del , CM000666.2:g.105542493_105542500del	GRCh38
NC_000004.11:g.106463650_106463657del , CM000666.1:g.106463650_106463657del	GRCh37
NC_000004.10:g.106683099_106683106del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.508_515del
XR_939039.1:n.668_675del
XR_939040.1:n.296-1021_296-1014del
XR_001741410.1:n.523_530del
XR_001741411.1:n.999_1006del
XR_001741412.1:n.449+74_449+81del
XR_001741413.1:n.523_530del
XR_001741414.1:n.449+74_449+81del
XR_939038.2:n.523_530del
XR_939040.2:n.311-1021_311-1014del