Canonical Allele Identifier: CA2343195894
Gene: GP6 HGNC NCBI
GP6-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55015615_55015619delinsCAAAG , CM000681.2:g.55015615_55015619delinsCAAAG GRCh38
NC_000019.8:g.60218795_60218799delinsCAAAG NCBI36
NG_031963.2:g.27646_27650delinsCTTTG , LRG_560:g.27646_27650delinsCTTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000310373.7:c.779+60_779+64delinsCTTTG (GP6) ENSP00000308782.3:n.779+60_779+64delinsCT...
ENST00000333884.2:c.721+64_721+68delinsCTTTG (GP6) ENSP00000334552.2:n.721+64_721+68delinsCT...
ENST00000417454.5:c.775+64_775+68delinsCTTTG (GP6) MANE Select ENSP00000394922.1:n.775+64_775+68delinsCT...
ENST00000465648.1:n.219+64_219+68delinsCTTTG (GP6)
NM_001083899.2:c.779+60_779+64delinsCTTTG , LRG_560t3:c.779+60_779+64delinsCTTTG (GP6) NP_001077368.2:n.779+60_779+64delinsCTTTG...
NM_001256017.2:c.721+64_721+68delinsCTTTG , LRG_560t2:c.721+64_721+68delinsCTTTG (GP6) NP_001242946.2:n.721+64_721+68delinsCTTTG...
NM_016363.5:c.775+64_775+68delinsCTTTG , LRG_560t1:c.775+64_775+68delinsCTTTG (GP6) MANE Select NP_057447.5:n.775+64_775+68delinsCTTTG
XR_001754012.2:n.312+9151_312+9155delinsCAAAG (GP6-AS1)
XR_001754013.2:n.305+9151_305+9155delinsCAAAG (GP6-AS1)
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