Canonical Allele Identifier: CA1694872881

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24282657_24282659delinsCCT , CM000669.2:g.24282657_24282659delinsCCT	GRCh38
NC_000007.13:g.24322276_24322278delinsCCT , CM000669.1:g.24322276_24322278delinsCCT	GRCh37
NC_000007.12:g.24288801_24288803delinsCCT	NCBI36
NG_016148.1:g.3470_3472delinsCCT

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-26960_42-26958delinsAGG	XP_016868399.1:n.42-26960_42-26958delinsAGG
XM_017012911.1:c.42-26960_42-26958delinsAGG	XP_016868400.1:n.42-26960_42-26958delinsAGG
XR_001745121.1:n.473+36698_473+36700delinsAGG
XR_001745122.1:n.345-85630_345-85628delinsAGG
XR_001745123.1:n.473+36698_473+36700delinsAGG
XR_001745124.1:n.473+36698_473+36700delinsAGG
XR_001745125.1:n.473+36698_473+36700delinsAGG
XR_001745126.1:n.473+36698_473+36700delinsAGG
XR_001745127.1:n.345-26960_345-26958delinsAGG
XR_001745129.1:n.473+36698_473+36700delinsAGG
XR_001745130.1:n.473+36698_473+36700delinsAGG
XR_001745131.1:n.473+36698_473+36700delinsAGG
XR_001745132.1:n.473+36698_473+36700delinsAGG