Canonical Allele Identifier: CA2728840864
Gene: GPC5 HGNC NCBI

Linked Data

dbSNP Id: rs2139205046

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.92670899T>C , CM000675.2:g.92670899T>C GRCh38
NC_000013.10:g.93323152T>C , CM000675.1:g.93323152T>C GRCh37
NC_000013.9:g.92121153T>C NCBI36
NG_009370.1:g.1277218T>C
NG_009370.2:g.1277219T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377067.9:c.1562-195383T>C MANE Select ENSP00000366267.3:n.1562-195383T>C
ENST00000377067.8:c.1562-195383T>C ENSP00000366267.3:n.1562-195383T>C
NM_004466.5:c.1562-195383T>C NP_004457.1:n.1562-195383T>C
XR_931643.1:n.173+6619A>G
XR_931644.1:n.173+6619A>G
XM_017020435.2:c.1562-79065T>C XP_016875924.1:n.1562-79065T>C
XR_931643.3:n.2210+6619A>G
XR_931644.2:n.2210+6619A>G
NM_004466.6:c.1562-195383T>C MANE Select NP_004457.1:n.1562-195383T>C