Canonical Allele Identifier: CA2652574752

Gene: GSS

Linked Data

• gnomAD v4: 20-34932179-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932179A>G , CM000682.2:g.34932179A>G	GRCh38
NC_000020.10:g.33519982A>G , CM000682.1:g.33519982A>G	GRCh37
NC_000020.9:g.32983643A>G	NCBI36
NG_008848.1:g.28620T>C
NG_008848.2:g.28849T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*475-46T>C	ENSP00000493524.1:n.*475-46T>C
ENST00000642498.1:c.835-46T>C	ENSP00000493631.1:n.835-46T>C
ENST00000642538.1:c.*179-46T>C	ENSP00000493927.1:n.*179-46T>C
ENST00000643188.1:c.835-46T>C	ENSP00000493903.1:n.835-46T>C
ENST00000643443.1:c.*542-46T>C	ENSP00000495572.1:n.*542-46T>C
ENST00000643502.1:c.492-46T>C
ENST00000643908.1:n.1053-46T>C
ENST00000644538.1:n.1112-46T>C
ENST00000644793.1:c.835-46T>C	ENSP00000495750.1:n.835-46T>C
ENST00000645328.1:c.213-46T>C
ENST00000645408.1:c.368-46T>C
ENST00000645723.1:n.2074-46T>C
ENST00000646405.1:c.*253-46T>C	ENSP00000493744.1:n.*253-46T>C
ENST00000646497.1:n.780-46T>C
ENST00000646512.1:n.981-46T>C
ENST00000646735.1:c.502-46T>C	ENSP00000493763.1:n.502-46T>C
ENST00000651619.1:c.835-46T>C MANE Select	ENSP00000498303.1:n.835-46T>C
ENST00000216951.6:c.835-46T>C	ENSP00000216951.2:n.835-46T>C
ENST00000451957.2:c.502-46T>C	ENSP00000407517.2:n.502-46T>C
NM_000178.2:c.835-46T>C	NP_000169.1:n.835-46T>C
XM_005260406.3:c.835-46T>C	XP_005260463.1:n.835-46T>C
XM_011528796.1:c.835-46T>C	XP_011527098.1:n.835-46T>C
NM_000178.4:c.835-46T>C MANE Select	NP_000169.1:n.835-46T>C
NM_001322494.1:c.835-46T>C	NP_001309423.1:n.835-46T>C
NM_001322495.1:c.835-46T>C	NP_001309424.1:n.835-46T>C