Canonical Allele Identifier: CA2576890585

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015677_55015679del , CM000681.2:g.55015677_55015679del GRCh38
NC_000019.8:g.60218857_60218859del NCBI36
NG_031963.2:g.27587_27589del , LRG_560:g.27587_27589del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310373.7:c.779+1_779+3del (GP6)
ENST00000333884.2:c.721+5_721+7del (GP6) ENSP00000334552.2:n.721+5_721+7del
ENST00000417454.5:c.775+5_775+7del (GP6) MANE Select ENSP00000394922.1:n.775+5_775+7del
ENST00000465648.1:n.219+5_219+7del (GP6)
NM_001083899.2:c.779+1_779+3del , LRG_560t3:c.779+1_779+3del (GP6)
NM_001256017.2:c.721+5_721+7del , LRG_560t2:c.721+5_721+7del (GP6) NP_001242946.2:n.721+5_721+7del
NM_016363.5:c.775+5_775+7del , LRG_560t1:c.775+5_775+7del (GP6) MANE Select NP_057447.5:n.775+5_775+7del
XR_001754012.2:n.312+9213_312+9215del (GP6-AS1)
XR_001754013.2:n.305+9213_305+9215del (GP6-AS1)