Canonical Allele Identifier: CA1694872912
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282726_24282727delinsAC , CM000669.2:g.24282726_24282727delinsAC GRCh38
NC_000007.13:g.24322345_24322346delinsAC , CM000669.1:g.24322345_24322346delinsAC GRCh37
NC_000007.12:g.24288870_24288871delinsAC NCBI36
NG_016148.1:g.3539_3540delinsAC

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27028_42-27027delinsGT XP_016868399.1:n.42-27028_42-27027delinsG...
XM_017012911.1:c.42-27028_42-27027delinsGT XP_016868400.1:n.42-27028_42-27027delinsG...
XR_001745121.1:n.473+36630_473+36631delinsGT
XR_001745122.1:n.345-85698_345-85697delinsGT
XR_001745123.1:n.473+36630_473+36631delinsGT
XR_001745124.1:n.473+36630_473+36631delinsGT
XR_001745125.1:n.473+36630_473+36631delinsGT
XR_001745126.1:n.473+36630_473+36631delinsGT
XR_001745127.1:n.345-27028_345-27027delinsGT
XR_001745129.1:n.473+36630_473+36631delinsGT
XR_001745130.1:n.473+36630_473+36631delinsGT
XR_001745131.1:n.473+36630_473+36631delinsGT
XR_001745132.1:n.473+36630_473+36631delinsGT