Canonical Allele Identifier: CA799758159

Gene:

Linked Data

• dbSNP Id: rs1254793552
• gnomAD v3: 4-89597799-T-TA
• gnomAD v4: 4-89597799-T-TA
• MyVariant Identifiers: chr4:g.90518950_90518951insA (hg19) ; chr4:g.89597799_89597800insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89597800dup , CM000666.2:g.89597800dup	GRCh38
NC_000004.11:g.90518951dup , CM000666.1:g.90518951dup	GRCh37
NC_000004.10:g.90737974dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+9860dup
XR_938987.1:n.433-353dup
XR_938988.1:n.299-353dup
XR_938990.1:n.298+9860dup
XR_938991.1:n.298+9860dup
XR_938992.1:n.298+9860dup
XR_938994.1:n.643+9860dup
XR_938995.1:n.477+9860dup
XR_938996.1:n.298+9860dup
XR_938997.1:n.298+9860dup
XR_938986.2:n.323+9860dup
XR_938987.2:n.493-353dup