Canonical Allele Identifier: CA2110972272
Gene: GPC5 HGNC NCBI

Linked Data

dbSNP Id: rs17267292

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.92670893T>A , CM000675.2:g.92670893T>A GRCh38
NC_000013.10:g.93323146T>A , CM000675.1:g.93323146T>A GRCh37
NC_000013.9:g.92121147T>A NCBI36
NG_009370.1:g.1277212T>A
NG_009370.2:g.1277213T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377067.9:c.1562-195389T>A MANE Select ENSP00000366267.3:n.1562-195389T>A
ENST00000377067.8:c.1562-195389T>A ENSP00000366267.3:n.1562-195389T>A
NM_004466.5:c.1562-195389T>A NP_004457.1:n.1562-195389T>A
XR_931643.1:n.173+6625A>T
XR_931644.1:n.173+6625A>T
XM_017020435.2:c.1562-79071T>A XP_016875924.1:n.1562-79071T>A
XR_931643.3:n.2210+6625A>T
XR_931644.2:n.2210+6625A>T
NM_004466.6:c.1562-195389T>A MANE Select NP_004457.1:n.1562-195389T>A