Canonical Allele Identifier: CA2111284163
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286362_93286365delinsCCTT , CM000675.2:g.93286362_93286365delinsCCTT GRCh38
NC_000013.10:g.93938615_93938618delinsCCTT , CM000675.1:g.93938615_93938618delinsCCTT GRCh37
NC_000013.9:g.92736616_92736619delinsCCTT NCBI36
NG_011880.1:g.64538_64541delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.160+58746_160+58749delinsCCTT MANE Select ENSP00000366246.3:n.160+58746_160+58749delinsCCTT
ENST00000377047.8:c.160+58746_160+58749delinsCCTT ENSP00000366246.3:n.160+58746_160+58749delinsCCTT
NM_005708.3:c.160+58746_160+58749delinsCCTT NP_005699.1:n.160+58746_160+58749delinsCCTT
NM_005708.4:c.160+58746_160+58749delinsCCTT NP_005699.1:n.160+58746_160+58749delinsCCTT
XM_017020299.2:c.-51+20405_-51+20408delinsCCTT XP_016875788.1:n.-51+20405_-51+20408delinsCCTT
NM_005708.5:c.160+58746_160+58749delinsCCTT MANE Select NP_005699.1:n.160+58746_160+58749delinsCCTT