Canonical Allele Identifier: CA2575435837
Gene: GPC6 HGNC NCBI
GPC6-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93830605del , CM000675.2:g.93830605del GRCh38
NC_000013.10:g.94482858del , CM000675.1:g.94482858del GRCh37
NC_000013.9:g.93280859del NCBI36
NG_011880.1:g.608781del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.711+60del (GPC6) MANE Select ENSP00000366246.3:n.711+60del
ENST00000377047.8:c.711+60del (GPC6) ENSP00000366246.3:n.711+60del
NM_005708.3:c.711+60del (GPC6) NP_005699.1:n.711+60del
NR_046536.1:n.380+212del (GPC6-AS2)
XM_011521044.1:c.501+60del (GPC6) XP_011519346.1:n.501+60del
NM_005708.4:c.711+60del (GPC6) NP_005699.1:n.711+60del
XM_011521044.2:c.501+60del (GPC6) XP_011519346.1:n.501+60del
XM_017020298.1:c.501+60del (GPC6) XP_016875787.1:n.501+60del
XM_017020299.2:c.501+60del (GPC6) XP_016875788.1:n.501+60del
XM_017020300.1:c.501+60del (GPC6) XP_016875789.1:n.501+60del
XM_017020301.1:c.345+60del (GPC6) XP_016875790.1:n.345+60del
NM_005708.5:c.711+60del (GPC6) MANE Select NP_005699.1:n.711+60del