Canonical Allele Identifier: CA2671644297
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542503_105542504insAGC , CM000666.2:g.105542503_105542504insAGC GRCh38
NC_000004.11:g.106463660_106463661insAGC , CM000666.1:g.106463660_106463661insAGC GRCh37
NC_000004.10:g.106683109_106683110insAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.502_503insCTG
XR_939039.1:n.662_663insCTG
XR_939040.1:n.296-1027_296-1026insCTG
XR_001741410.1:n.517_518insCTG
XR_001741411.1:n.993_994insCTG
XR_001741412.1:n.449+68_449+69insCTG
XR_001741413.1:n.517_518insCTG
XR_001741414.1:n.449+68_449+69insCTG
XR_939038.2:n.517_518insCTG
XR_939040.2:n.311-1027_311-1026insCTG