Canonical Allele Identifier: CA1099401424

Gene:

Linked Data

• dbSNP Id: rs1787632560
• gnomAD v3: 7-24291886-CT-C
• gnomAD v4: 7-24291886-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291887del , CM000669.2:g.24291887del	GRCh38
NC_000007.13:g.24331506del , CM000669.1:g.24331506del	GRCh37
NC_000007.12:g.24298031del	NCBI36
NG_016148.1:g.12700del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.41+27470del	XP_016868399.1:n.41+27470del
XM_017012911.1:c.41+27470del	XP_016868400.1:n.41+27470del
XR_001745121.1:n.473+27470del
XR_001745122.1:n.345-94858del
XR_001745123.1:n.473+27470del
XR_001745124.1:n.473+27470del
XR_001745125.1:n.473+27470del
XR_001745126.1:n.473+27470del
XR_001745127.1:n.345-36188del
XR_001745129.1:n.473+27470del
XR_001745130.1:n.473+27470del
XR_001745131.1:n.473+27470del
XR_001745132.1:n.473+27470del