Canonical Allele Identifier: CA1694872921
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282739_24282740delinsTC , CM000669.2:g.24282739_24282740delinsTC GRCh38
NC_000007.13:g.24322358_24322359delinsTC , CM000669.1:g.24322358_24322359delinsTC GRCh37
NC_000007.12:g.24288883_24288884delinsTC NCBI36
NG_016148.1:g.3552_3553delinsTC

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27041_42-27040delinsGA XP_016868399.1:n.42-27041_42-27040delinsG...
XM_017012911.1:c.42-27041_42-27040delinsGA XP_016868400.1:n.42-27041_42-27040delinsG...
XR_001745121.1:n.473+36617_473+36618delinsGA
XR_001745122.1:n.345-85711_345-85710delinsGA
XR_001745123.1:n.473+36617_473+36618delinsGA
XR_001745124.1:n.473+36617_473+36618delinsGA
XR_001745125.1:n.473+36617_473+36618delinsGA
XR_001745126.1:n.473+36617_473+36618delinsGA
XR_001745127.1:n.345-27041_345-27040delinsGA
XR_001745129.1:n.473+36617_473+36618delinsGA
XR_001745130.1:n.473+36617_473+36618delinsGA
XR_001745131.1:n.473+36617_473+36618delinsGA
XR_001745132.1:n.473+36617_473+36618delinsGA