Canonical Allele Identifier: CA408701116

Gene: GSS

Linked Data

• dbSNP Id: rs1304810463
• gnomAD v2: 20-33519800-T-G
• gnomAD v4: 20-34931997-T-G
• MyVariant Identifiers: chr20:g.33519800T>G (hg19) ; chr20:g.34931997T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931997T>G , CM000682.2:g.34931997T>G	GRCh38
NC_000020.10:g.33519800T>G , CM000682.1:g.33519800T>G	GRCh37
NC_000020.9:g.32983461T>G	NCBI36
NG_008848.1:g.28802A>C
NG_008848.2:g.29031A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.971A>C	ENSP00000493631.1:p.Gln324Pro
ENST00000642538.1:c.*315A>C	ENSP00000493927.1:n.*315A>C
ENST00000643188.1:c.971A>C	ENSP00000493903.1:p.Gln324Pro
ENST00000643443.1:c.*678A>C	ENSP00000495572.1:n.*678A>C
ENST00000643502.1:c.628A>C
ENST00000643908.1:n.1189A>C
ENST00000644538.1:n.1248A>C
ENST00000644793.1:c.971A>C	ENSP00000495750.1:p.Gln324Pro
ENST00000645328.1:c.349A>C
ENST00000645408.1:c.504A>C
ENST00000645723.1:n.2210A>C
ENST00000646405.1:c.*389A>C	ENSP00000493744.1:n.*389A>C
ENST00000646512.1:n.1117A>C
ENST00000646735.1:c.638A>C	ENSP00000493763.1:p.Gln213Pro
ENST00000651619.1:c.971A>C MANE Select	ENSP00000498303.1:p.Gln324Pro
ENST00000216951.6:c.971A>C	ENSP00000216951.2:p.Gln324Pro
ENST00000451957.2:c.638A>C	ENSP00000407517.2:p.Gln213Pro
NM_000178.2:c.971A>C	NP_000169.1:p.Gln324Pro
XM_005260406.3:c.971A>C	XP_005260463.1:p.Gln324Pro
XM_011528796.1:c.971A>C	XP_011527098.1:p.Gln324Pro
NM_000178.4:c.971A>C MANE Select	NP_000169.1:p.Gln324Pro
NM_001322494.1:c.971A>C	NP_001309423.1:p.Gln324Pro
NM_001322495.1:c.971A>C	NP_001309424.1:p.Gln324Pro