Canonical Allele Identifier: CA799758327

Gene:

Linked Data

• dbSNP Id: rs1263898417
• gnomAD v3: 4-89598047-GTT-G
• gnomAD v4: 4-89598047-GTT-G
• MyVariant Identifiers: chr4:g.90519199_90519200del (hg19) ; chr4:g.89598048_89598049del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89598050_89598051del , CM000666.2:g.89598050_89598051del	GRCh38
NC_000004.11:g.90519201_90519202del , CM000666.1:g.90519201_90519202del	GRCh37
NC_000004.10:g.90738224_90738225del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+10110_298+10111del
XR_938987.1:n.433-103_433-102del
XR_938988.1:n.299-103_299-102del
XR_938990.1:n.298+10110_298+10111del
XR_938991.1:n.298+10110_298+10111del
XR_938992.1:n.298+10110_298+10111del
XR_938994.1:n.643+10110_643+10111del
XR_938995.1:n.477+10110_477+10111del
XR_938996.1:n.298+10110_298+10111del
XR_938997.1:n.298+10110_298+10111del
XR_938986.2:n.323+10110_323+10111del
XR_938987.2:n.493-103_493-102del