Canonical Allele Identifier: CA254867176

Gene: GPC5

Linked Data

• dbSNP Id: rs572447707
• gnomAD v3: 13-92670901-G-C
• gnomAD v4: 13-92670901-G-C
• MyVariant Identifiers: chr13:g.93323154G>C (hg19) ; chr13:g.92670901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.92670901G>C , CM000675.2:g.92670901G>C	GRCh38
NC_000013.10:g.93323154G>C , CM000675.1:g.93323154G>C	GRCh37
NC_000013.9:g.92121155G>C	NCBI36
NG_009370.1:g.1277220G>C
NG_009370.2:g.1277221G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377067.9:c.1562-195381G>C MANE Select	ENSP00000366267.3:n.1562-195381G>C
ENST00000377067.8:c.1562-195381G>C	ENSP00000366267.3:n.1562-195381G>C
NM_004466.5:c.1562-195381G>C	NP_004457.1:n.1562-195381G>C
XR_931643.1:n.173+6617C>G
XR_931644.1:n.173+6617C>G
XM_017020435.2:c.1562-79063G>C	XP_016875924.1:n.1562-79063G>C
XR_931643.3:n.2210+6617C>G
XR_931644.2:n.2210+6617C>G
NM_004466.6:c.1562-195381G>C MANE Select	NP_004457.1:n.1562-195381G>C