Canonical Allele Identifier: CA2111284170
Gene: GPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286386A= , CM000675.2:g.93286386A= GRCh38
NC_000013.10:g.93938639A= , CM000675.1:g.93938639A= GRCh37
NC_000013.9:g.92736640A= NCBI36
NG_011880.1:g.64562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.160+58770A= MANE Select ENSP00000366246.3:n.160+58770A=
ENST00000377047.8:c.160+58770A= ENSP00000366246.3:n.160+58770A=
NM_005708.3:c.160+58770A= NP_005699.1:n.160+58770A=
NM_005708.4:c.160+58770A= NP_005699.1:n.160+58770A=
XM_017020299.2:c.-51+20429A= XP_016875788.1:n.-51+20429A=
NM_005708.5:c.160+58770A= MANE Select NP_005699.1:n.160+58770A=