Canonical Allele Identifier: CA408704330

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33530337A>G (hg19) ; chr20:g.34942534A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34942534A>G , CM000682.2:g.34942534A>G	GRCh38
NC_000020.10:g.33530337A>G , CM000682.1:g.33530337A>G	GRCh37
NC_000020.9:g.32993998A>G	NCBI36
NG_008848.1:g.18265T>C
NG_008848.2:g.18494T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*152T>C	ENSP00000493524.1:n.*152T>C
ENST00000642498.1:c.445T>C	ENSP00000493631.1:p.Ser149Pro
ENST00000642538.1:c.351+397T>C	ENSP00000493927.1:n.351+397T>C
ENST00000643188.1:c.445T>C	ENSP00000493903.1:p.Ser149Pro
ENST00000643443.1:c.*152T>C	ENSP00000495572.1:n.*152T>C
ENST00000643502.1:c.102T>C
ENST00000643908.1:n.808T>C
ENST00000644538.1:n.722T>C
ENST00000644793.1:c.445T>C	ENSP00000495750.1:p.Ser149Pro
ENST00000645408.1:c.45T>C
ENST00000645723.1:n.1684T>C
ENST00000646405.1:c.351+397T>C	ENSP00000493744.1:n.351+397T>C
ENST00000646497.1:n.392T>C
ENST00000646502.1:n.927T>C
ENST00000646512.1:n.658T>C
ENST00000646735.1:c.275+3419T>C	ENSP00000493763.1:n.275+3419T>C
ENST00000646766.1:c.*75T>C	ENSP00000494333.1:n.*75T>C
ENST00000651619.1:c.445T>C MANE Select	ENSP00000498303.1:p.Ser149Pro
ENST00000216951.6:c.445T>C	ENSP00000216951.2:p.Ser149Pro
ENST00000451957.2:c.275+3419T>C	ENSP00000407517.2:n.275+3419T>C
NM_000178.2:c.445T>C	NP_000169.1:p.Ser149Pro
XM_005260406.3:c.445T>C	XP_005260463.1:p.Ser149Pro
XM_011528796.1:c.445T>C	XP_011527098.1:p.Ser149Pro
NM_000178.4:c.445T>C MANE Select	NP_000169.1:p.Ser149Pro
NM_001322494.1:c.445T>C	NP_001309423.1:p.Ser149Pro
NM_001322495.1:c.445T>C	NP_001309424.1:p.Ser149Pro