Canonical Allele Identifier: CA2343195927

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015688_55015690delinsGGA , CM000681.2:g.55015688_55015690delinsGGA GRCh38
NC_000019.8:g.60218868_60218870delinsGGA NCBI36
NG_031963.2:g.27575_27577delinsTCC , LRG_560:g.27575_27577delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.768_770delinsTCC (GP6) ENSP00000308782.3:p.Ser256=
ENST00000333884.2:c.714_716delinsTCC (GP6) ENSP00000334552.2:p.Ser238=
ENST00000417454.5:c.768_770delinsTCC (GP6) MANE Select ENSP00000394922.1:p.Ser256=
ENST00000465648.1:n.212_214delinsTCC (GP6)
NM_001083899.2:c.768_770delinsTCC , LRG_560t3:c.768_770delinsTCC (GP6) NP_001077368.2:p.Ser256=
NM_001256017.2:c.714_716delinsTCC , LRG_560t2:c.714_716delinsTCC (GP6) NP_001242946.2:p.Ser238=
NM_016363.5:c.768_770delinsTCC , LRG_560t1:c.768_770delinsTCC (GP6) MANE Select NP_057447.5:p.Ser256=
XR_001754012.2:n.312+9224_312+9226delinsGGA (GP6-AS1)
XR_001754013.2:n.305+9224_305+9226delinsGGA (GP6-AS1)