Canonical Allele Identifier: CA1694873174

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283306_24283308delinsCTG , CM000669.2:g.24283306_24283308delinsCTG	GRCh38
NC_000007.13:g.24322925_24322927delinsCTG , CM000669.1:g.24322925_24322927delinsCTG	GRCh37
NC_000007.12:g.24289450_24289452delinsCTG	NCBI36
NG_016148.1:g.4119_4121delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27609_42-27607delinsCAG	XP_016868399.1:n.42-27609_42-27607delinsCAG
XM_017012911.1:c.42-27609_42-27607delinsCAG	XP_016868400.1:n.42-27609_42-27607delinsCAG
XR_001745121.1:n.473+36049_473+36051delinsCAG
XR_001745122.1:n.345-86279_345-86277delinsCAG
XR_001745123.1:n.473+36049_473+36051delinsCAG
XR_001745124.1:n.473+36049_473+36051delinsCAG
XR_001745125.1:n.473+36049_473+36051delinsCAG
XR_001745126.1:n.473+36049_473+36051delinsCAG
XR_001745127.1:n.345-27609_345-27607delinsCAG
XR_001745129.1:n.473+36049_473+36051delinsCAG
XR_001745130.1:n.473+36049_473+36051delinsCAG
XR_001745131.1:n.473+36049_473+36051delinsCAG
XR_001745132.1:n.473+36049_473+36051delinsCAG