Canonical Allele Identifier: CA13850011
Gene: GPC5 HGNC NCBI

Linked Data

dbSNP Id: rs1413191

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.92561223C>T , CM000675.2:g.92561223C>T GRCh38
NC_000013.10:g.93213476C>T , CM000675.1:g.93213476C>T GRCh37
NC_000013.9:g.92011477C>T NCBI36
NG_009370.1:g.1167542C>T
NG_009370.2:g.1167543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377067.9:c.1562-305059C>T MANE Select ENSP00000366267.3:n.1562-305059C>T
ENST00000377067.8:c.1562-305059C>T ENSP00000366267.3:n.1562-305059C>T
NM_004466.5:c.1562-305059C>T NP_004457.1:n.1562-305059C>T
XM_017020435.2:c.1562-188741C>T XP_016875924.1:n.1562-188741C>T
NM_004466.6:c.1562-305059C>T MANE Select NP_004457.1:n.1562-305059C>T