Canonical Allele Identifier: CA408701002

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519741C>G (hg19) ; chr20:g.34931938C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931938C>G , CM000682.2:g.34931938C>G	GRCh38
NC_000020.10:g.33519741C>G , CM000682.1:g.33519741C>G	GRCh37
NC_000020.9:g.32983402C>G	NCBI36
NG_008848.1:g.28861G>C
NG_008848.2:g.29090G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.1029+1G>C	ENSP00000493631.1:n.1029+1G>C
ENST00000642538.1:c.*373+1G>C	ENSP00000493927.1:n.*373+1G>C
ENST00000643188.1:c.1029+1G>C	ENSP00000493903.1:n.1029+1G>C
ENST00000643443.1:c.*736+1G>C	ENSP00000495572.1:n.*736+1G>C
ENST00000643502.1:c.686+1G>C
ENST00000643908.1:n.1247+1G>C
ENST00000644538.1:n.1306+1G>C
ENST00000644793.1:c.1029+1G>C	ENSP00000495750.1:n.1029+1G>C
ENST00000645328.1:c.407+1G>C
ENST00000645408.1:c.562+1G>C
ENST00000645723.1:n.2268+1G>C
ENST00000646405.1:c.*447+1G>C	ENSP00000493744.1:n.*447+1G>C
ENST00000646512.1:n.1175+1G>C
ENST00000646735.1:c.696+1G>C	ENSP00000493763.1:n.696+1G>C
ENST00000651619.1:c.1029+1G>C MANE Select	ENSP00000498303.1:n.1029+1G>C
ENST00000216951.6:c.1029+1G>C	ENSP00000216951.2:n.1029+1G>C
ENST00000451957.2:c.696+1G>C	ENSP00000407517.2:n.696+1G>C
NM_000178.2:c.1029+1G>C	NP_000169.1:n.1029+1G>C
XM_005260406.3:c.1029+1G>C	XP_005260463.1:n.1029+1G>C
XM_011528796.1:c.1029+1G>C	XP_011527098.1:n.1029+1G>C
NM_000178.4:c.1029+1G>C MANE Select	NP_000169.1:n.1029+1G>C
NM_001322494.1:c.1029+1G>C	NP_001309423.1:n.1029+1G>C
NM_001322495.1:c.1029+1G>C	NP_001309424.1:n.1029+1G>C