Canonical Allele Identifier: CA2587209007

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015727_55015728del , CM000681.2:g.55015727_55015728del GRCh38
NC_000019.8:g.60218907_60218908del NCBI36
NG_031963.2:g.27538_27539del , LRG_560:g.27538_27539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.731_732del (GP6) ENSP00000308782.3:p.Ser244Ter
ENST00000333884.2:c.677_678del (GP6) ENSP00000334552.2:p.Ser226Ter
ENST00000417454.5:c.731_732del (GP6) MANE Select ENSP00000394922.1:p.Ser244Ter
ENST00000465648.1:n.175_176del (GP6)
NM_001083899.2:c.731_732del , LRG_560t3:c.731_732del (GP6) NP_001077368.2:p.Ser244Ter
NM_001256017.2:c.677_678del , LRG_560t2:c.677_678del (GP6) NP_001242946.2:p.Ser226Ter
NM_016363.5:c.731_732del , LRG_560t1:c.731_732del (GP6) MANE Select NP_057447.5:p.Ser244Ter
XR_001754012.2:n.312+9263_312+9264del (GP6-AS1)
XR_001754013.2:n.305+9263_305+9264del (GP6-AS1)