Canonical Allele Identifier: CA883669513

Linked Data

dbSNP Id: rs1457504107

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015764_55015768dup , CM000681.2:g.55015764_55015768dup GRCh38
NC_000019.8:g.60218944_60218948dup NCBI36
NG_031963.2:g.27502_27506dup , LRG_560:g.27502_27506dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.725-30_725-26dup (GP6) ENSP00000308782.3:n.725-30_725-26dup
ENST00000333884.2:c.671-30_671-26dup (GP6) ENSP00000334552.2:n.671-30_671-26dup
ENST00000417454.5:c.725-30_725-26dup (GP6) MANE Select ENSP00000394922.1:n.725-30_725-26dup
ENST00000465648.1:n.169-30_169-26dup (GP6)
NM_001083899.2:c.725-30_725-26dup , LRG_560t3:c.725-30_725-26dup (GP6) NP_001077368.2:n.725-30_725-26dup
NM_001256017.2:c.671-30_671-26dup , LRG_560t2:c.671-30_671-26dup (GP6) NP_001242946.2:n.671-30_671-26dup
NM_016363.5:c.725-30_725-26dup , LRG_560t1:c.725-30_725-26dup (GP6) MANE Select NP_057447.5:n.725-30_725-26dup
XR_001754012.2:n.312+9300_312+9304dup (GP6-AS1)
XR_001754013.2:n.305+9300_305+9304dup (GP6-AS1)