Canonical Allele Identifier: CA155828805

Gene:

Linked Data

• dbSNP Id: rs893287266
• gnomAD v3: 7-24283406-C-CT
• gnomAD v4: 7-24283406-C-CT
• MyVariant Identifiers: chr7:g.24323025_24323026insT (hg19) ; chr7:g.24283406_24283407insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283411dup , CM000669.2:g.24283411dup	GRCh38
NC_000007.13:g.24323030dup , CM000669.1:g.24323030dup	GRCh37
NC_000007.12:g.24289555dup	NCBI36
NG_016148.1:g.4224dup

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27708dup	XP_016868399.1:n.42-27708dup
XM_017012911.1:c.42-27708dup	XP_016868400.1:n.42-27708dup
XR_001745121.1:n.473+35950dup
XR_001745122.1:n.345-86378dup
XR_001745123.1:n.473+35950dup
XR_001745124.1:n.473+35950dup
XR_001745125.1:n.473+35950dup
XR_001745126.1:n.473+35950dup
XR_001745127.1:n.345-27708dup
XR_001745129.1:n.473+35950dup
XR_001745130.1:n.473+35950dup
XR_001745131.1:n.473+35950dup
XR_001745132.1:n.473+35950dup