Canonical Allele Identifier: CA2814871219

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015816_55015853del , CM000681.2:g.55015816_55015853del GRCh38
NC_000019.8:g.60218996_60219033del NCBI36
NG_031963.2:g.27414_27451del , LRG_560:g.27414_27451del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.725-118_725-81del (GP6) ENSP00000308782.3:n.725-118_725-81del
ENST00000333884.2:c.671-118_671-81del (GP6) ENSP00000334552.2:n.671-118_671-81del
ENST00000417454.5:c.725-118_725-81del (GP6) MANE Select ENSP00000394922.1:n.725-118_725-81del
ENST00000465648.1:n.169-118_169-81del (GP6)
NM_001083899.2:c.725-118_725-81del , LRG_560t3:c.725-118_725-81del (GP6) NP_001077368.2:n.725-118_725-81del
NM_001256017.2:c.671-118_671-81del , LRG_560t2:c.671-118_671-81del (GP6) NP_001242946.2:n.671-118_671-81del
NM_016363.5:c.725-118_725-81del , LRG_560t1:c.725-118_725-81del (GP6) MANE Select NP_057447.5:n.725-118_725-81del
XR_001754012.2:n.312+9352_312+9389del (GP6-AS1)
XR_001754013.2:n.305+9352_305+9389del (GP6-AS1)