Canonical Allele Identifier: CA254867175

Gene: GPC5

Linked Data

• dbSNP Id: rs1007376114
• gnomAD v3: 13-92670892-C-CT
• gnomAD v4: 13-92670892-C-CT
• MyVariant Identifiers: chr13:g.93323145_93323146insT (hg19) ; chr13:g.92670892_92670893insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.92670897dup , CM000675.2:g.92670897dup	GRCh38
NC_000013.10:g.93323150dup , CM000675.1:g.93323150dup	GRCh37
NC_000013.9:g.92121151dup	NCBI36
NG_009370.1:g.1277216dup
NG_009370.2:g.1277217dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000377067.9:c.1562-195385dup MANE Select	ENSP00000366267.3:n.1562-195385dup
ENST00000377067.8:c.1562-195385dup	ENSP00000366267.3:n.1562-195385dup
NM_004466.5:c.1562-195385dup	NP_004457.1:n.1562-195385dup
XR_931643.1:n.173+6625dup
XR_931644.1:n.173+6625dup
XM_017020435.2:c.1562-79067dup	XP_016875924.1:n.1562-79067dup
XR_931643.3:n.2210+6625dup
XR_931644.2:n.2210+6625dup
NM_004466.6:c.1562-195385dup MANE Select	NP_004457.1:n.1562-195385dup