Canonical Allele Identifier: CA254829469

Gene: GPC5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.92336070C>A , CM000675.2:g.92336070C>A	GRCh38
NC_000013.10:g.92988323C>A , CM000675.1:g.92988323C>A	GRCh37
NC_000013.9:g.91786324C>A	NCBI36
NG_009370.1:g.942389C>A
NG_009370.2:g.942390C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377067.9:c.1561+191081C>A MANE Select	ENSP00000366267.3:n.1561+191081C>A
ENST00000377067.8:c.1561+191081C>A	ENSP00000366267.3:n.1561+191081C>A
NM_004466.5:c.1561+191081C>A	NP_004457.1:n.1561+191081C>A
XM_017020435.2:c.1561+191081C>A	XP_016875924.1:n.1561+191081C>A
NM_004466.6:c.1561+191081C>A MANE Select	NP_004457.1:n.1561+191081C>A