Canonical Allele Identifier: CA2110972289
Gene: GPC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.92670909G= , CM000675.2:g.92670909G= GRCh38
NC_000013.10:g.93323162G= , CM000675.1:g.93323162G= GRCh37
NC_000013.9:g.92121163G= NCBI36
NG_009370.1:g.1277228G=
NG_009370.2:g.1277229G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377067.9:c.1562-195373G= MANE Select ENSP00000366267.3:n.1562-195373G=
ENST00000377067.8:c.1562-195373G= ENSP00000366267.3:n.1562-195373G=
NM_004466.5:c.1562-195373G= NP_004457.1:n.1562-195373G=
XR_931643.1:n.173+6609C=
XR_931644.1:n.173+6609C=
XM_017020435.2:c.1562-79055G= XP_016875924.1:n.1562-79055G=
XR_931643.3:n.2210+6609C=
XR_931644.2:n.2210+6609C=
NM_004466.6:c.1562-195373G= MANE Select NP_004457.1:n.1562-195373G=