Canonical Allele Identifier: CA2110972362
Gene: GPC5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.92670950T= , CM000675.2:g.92670950T= GRCh38
NC_000013.10:g.93323203T= , CM000675.1:g.93323203T= GRCh37
NC_000013.9:g.92121204T= NCBI36
NG_009370.1:g.1277269T=
NG_009370.2:g.1277270T=

Transcript Alleles

HGVS Amino-acid change
ENST00000377067.9:c.1562-195332T= MANE Select ENSP00000366267.3:n.1562-195332T=
ENST00000377067.8:c.1562-195332T= ENSP00000366267.3:n.1562-195332T=
NM_004466.5:c.1562-195332T= NP_004457.1:n.1562-195332T=
XR_931643.1:n.173+6568A=
XR_931644.1:n.173+6568A=
XM_017020435.2:c.1562-79014T= XP_016875924.1:n.1562-79014T=
XR_931643.3:n.2210+6568A=
XR_931644.2:n.2210+6568A=
NM_004466.6:c.1562-195332T= MANE Select NP_004457.1:n.1562-195332T=
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