Canonical Allele Identifier: CA254969610

Gene: GPC6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93556396A>G , CM000675.2:g.93556396A>G	GRCh38
NC_000013.10:g.94208649A>G , CM000675.1:g.94208649A>G	GRCh37
NC_000013.9:g.93006650A>G	NCBI36
NG_011880.1:g.334572A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.319+10975A>G MANE Select	ENSP00000366246.3:n.319+10975A>G
ENST00000377047.8:c.319+10975A>G	ENSP00000366246.3:n.319+10975A>G
NM_005708.3:c.319+10975A>G	NP_005699.1:n.319+10975A>G
XM_011521044.1:c.109+10975A>G	XP_011519346.1:n.109+10975A>G
NM_005708.4:c.319+10975A>G	NP_005699.1:n.319+10975A>G
XM_011521044.2:c.109+10975A>G	XP_011519346.1:n.109+10975A>G
XM_017020298.1:c.109+10975A>G	XP_016875787.1:n.109+10975A>G
XM_017020299.2:c.109+10975A>G	XP_016875788.1:n.109+10975A>G
XM_017020300.1:c.109+10975A>G	XP_016875789.1:n.109+10975A>G
NM_005708.5:c.319+10975A>G MANE Select	NP_005699.1:n.319+10975A>G