Canonical Allele Identifier: CA2111284169
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286380G= , CM000675.2:g.93286380G= GRCh38
NC_000013.10:g.93938633G= , CM000675.1:g.93938633G= GRCh37
NC_000013.9:g.92736634G= NCBI36
NG_011880.1:g.64556G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.160+58764G= MANE Select ENSP00000366246.3:n.160+58764G=
ENST00000377047.8:c.160+58764G= ENSP00000366246.3:n.160+58764G=
NM_005708.3:c.160+58764G= NP_005699.1:n.160+58764G=
NM_005708.4:c.160+58764G= NP_005699.1:n.160+58764G=
XM_017020299.2:c.-51+20423G= XP_016875788.1:n.-51+20423G=
NM_005708.5:c.160+58764G= MANE Select NP_005699.1:n.160+58764G=