Canonical Allele Identifier: CA367637009

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425906A>G (hg19) ; chr7:g.65960919A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960919A>G , CM000669.2:g.65960919A>G	GRCh38
NC_000007.13:g.65425906A>G , CM000669.1:g.65425906A>G	GRCh37
NC_000007.12:g.65063341A>G	NCBI36
NG_016197.1:g.26396T>C
NG_051954.1:g.92821A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1934T>C MANE Select	ENSP00000302728.4:p.Leu645Ser
ENST00000304895.8:c.1934T>C	ENSP00000302728.4:p.Leu645Ser
ENST00000421103.5:c.1496T>C	ENSP00000391390.1:p.Leu499Ser
ENST00000430730.5:c.*1201T>C	ENSP00000411859.1:n.*1201T>C
ENST00000447929.5:c.*1314T>C	ENSP00000411262.1:n.*1314T>C
ENST00000466883.5:n.2324T>C
NM_000181.3:c.1934T>C	NP_000172.2:p.Leu645Ser
NM_001284290.1:c.1496T>C	NP_001271219.1:p.Leu499Ser
NM_001293104.1:c.1364T>C	NP_001280033.1:p.Leu455Ser
NM_001293105.1:c.1277T>C	NP_001280034.1:p.Leu426Ser
NR_120531.1:n.1980T>C
XM_005250297.3:c.1781T>C	XP_005250354.1:p.Leu594Ser
XM_011516113.1:c.1433T>C	XP_011514415.1:p.Leu478Ser
XM_011516114.1:c.1262T>C	XP_011514416.1:p.Leu421Ser
XM_005250297.4:c.1781T>C	XP_005250354.1:p.Leu594Ser
XM_011516114.2:c.1262T>C	XP_011514416.1:p.Leu421Ser
XM_017012091.1:c.1280T>C	XP_016867580.1:p.Leu427Ser
XM_017012092.1:c.1211T>C	XP_016867581.1:p.Leu404Ser
XM_017012093.2:c.1109T>C	XP_016867582.1:p.Leu370Ser
XR_001744658.2:n.1741T>C
XR_001744659.2:n.1854T>C
XR_001744660.2:n.1786T>C
XR_001744661.2:n.1701T>C
XR_927461.3:n.1939T>C
NM_000181.4:c.1934T>C MANE Select	NP_000172.2:p.Leu645Ser
NM_001284290.2:c.1496T>C	NP_001271219.1:p.Leu499Ser
NM_001293104.2:c.1364T>C	NP_001280033.1:p.Leu455Ser
NM_001293105.2:c.1277T>C	NP_001280034.1:p.Leu426Ser
NR_120531.2:n.1879T>C