Canonical Allele Identifier: CA15787601

Gene: GPC6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.94300578T>C , CM000675.2:g.94300578T>C	GRCh38
NC_000013.10:g.94952832T>C , CM000675.1:g.94952832T>C	GRCh37
NC_000013.9:g.93750833T>C	NCBI36
NG_011880.1:g.1078755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.1009-5402T>C MANE Select	ENSP00000366246.3:n.1009-5402T>C
ENST00000377047.8:c.1009-5402T>C	ENSP00000366246.3:n.1009-5402T>C
ENST00000617456.1:c.133-5402T>C	ENSP00000477667.1:n.133-5402T>C
NM_005708.3:c.1009-5402T>C	NP_005699.1:n.1009-5402T>C
XM_011521044.1:c.799-5402T>C	XP_011519346.1:n.799-5402T>C
NM_005708.4:c.1009-5402T>C	NP_005699.1:n.1009-5402T>C
XM_011521044.2:c.799-5402T>C	XP_011519346.1:n.799-5402T>C
XM_017020298.1:c.799-5402T>C	XP_016875787.1:n.799-5402T>C
XM_017020299.2:c.799-5402T>C	XP_016875788.1:n.799-5402T>C
XM_017020300.1:c.799-5402T>C	XP_016875789.1:n.799-5402T>C
XM_017020301.1:c.643-5402T>C	XP_016875790.1:n.643-5402T>C
XM_017020302.1:c.316-5402T>C	XP_016875791.1:n.316-5402T>C
NM_005708.5:c.1009-5402T>C MANE Select	NP_005699.1:n.1009-5402T>C