Canonical Allele Identifier: CA13850176

Gene: GPC6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93580876A>C , CM000675.2:g.93580876A>C	GRCh38
NC_000013.10:g.94233129A>C , CM000675.1:g.94233129A>C	GRCh37
NC_000013.9:g.93031130A>C	NCBI36
NG_011880.1:g.359052A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.319+35455A>C MANE Select	ENSP00000366246.3:n.319+35455A>C
ENST00000377047.8:c.319+35455A>C	ENSP00000366246.3:n.319+35455A>C
NM_005708.3:c.319+35455A>C	NP_005699.1:n.319+35455A>C
XM_011521044.1:c.109+35455A>C	XP_011519346.1:n.109+35455A>C
NM_005708.4:c.319+35455A>C	NP_005699.1:n.319+35455A>C
XM_011521044.2:c.109+35455A>C	XP_011519346.1:n.109+35455A>C
XM_017020298.1:c.109+35455A>C	XP_016875787.1:n.109+35455A>C
XM_017020299.2:c.109+35455A>C	XP_016875788.1:n.109+35455A>C
XM_017020300.1:c.109+35455A>C	XP_016875789.1:n.109+35455A>C
NM_005708.5:c.319+35455A>C MANE Select	NP_005699.1:n.319+35455A>C