Canonical Allele Identifier: CA2111458421
Community Standard Title: NM_005708.5(GPC6):c.319+35455A=
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93580876A= , CM000675.2:g.93580876A= GRCh38
NC_000013.10:g.94233129A= , CM000675.1:g.94233129A= GRCh37
NC_000013.9:g.93031130A= NCBI36
NG_011880.1:g.359052A=

Transcript Alleles

HGVS Amino-acid Change
NM_005708.5:c.319+35455A= MANE Select NP_005699.1:n.319+35455A=
ENST00000377047.9:c.319+35455A= MANE Select ENSP00000366246.3:n.319+35455A=
NM_005708.3:c.319+35455A= NP_005699.1:n.319+35455A=
NM_005708.4:c.319+35455A= NP_005699.1:n.319+35455A=
ENST00000377047.8:c.319+35455A= ENSP00000366246.3:n.319+35455A=
XM_011521044.1:c.109+35455A= XP_011519346.1:n.109+35455A=
XM_011521044.2:c.109+35455A= XP_011519346.1:n.109+35455A=
XM_017020298.1:c.109+35455A= XP_016875787.1:n.109+35455A=
XM_017020299.2:c.109+35455A= XP_016875788.1:n.109+35455A=
XM_017020300.1:c.109+35455A= XP_016875789.1:n.109+35455A=