Canonical Allele Identifier: CA702413224

Gene: GPC6

Linked Data

• dbSNP Id: rs1160879393
• MyVariant Identifiers: chr13:g.93938608G>T (hg19) ; chr13:g.93286355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.93286355G>T , CM000675.2:g.93286355G>T	GRCh38
NC_000013.10:g.93938608G>T , CM000675.1:g.93938608G>T	GRCh37
NC_000013.9:g.92736609G>T	NCBI36
NG_011880.1:g.64531G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377047.9:c.160+58739G>T MANE Select	ENSP00000366246.3:n.160+58739G>T
ENST00000377047.8:c.160+58739G>T	ENSP00000366246.3:n.160+58739G>T
NM_005708.3:c.160+58739G>T	NP_005699.1:n.160+58739G>T
NM_005708.4:c.160+58739G>T	NP_005699.1:n.160+58739G>T
XM_017020299.2:c.-51+20398G>T	XP_016875788.1:n.-51+20398G>T
NM_005708.5:c.160+58739G>T MANE Select	NP_005699.1:n.160+58739G>T