Canonical Allele Identifier: CA367637018

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425909C>G (hg19) ; chr7:g.65960922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960922C>G , CM000669.2:g.65960922C>G	GRCh38
NC_000007.13:g.65425909C>G , CM000669.1:g.65425909C>G	GRCh37
NC_000007.12:g.65063344C>G	NCBI36
NG_016197.1:g.26393G>C
NG_051954.1:g.92824C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1931G>C MANE Select	ENSP00000302728.4:p.Cys644Ser
ENST00000304895.8:c.1931G>C	ENSP00000302728.4:p.Cys644Ser
ENST00000421103.5:c.1493G>C	ENSP00000391390.1:p.Cys498Ser
ENST00000430730.5:c.*1198G>C	ENSP00000411859.1:n.*1198G>C
ENST00000447929.5:c.*1311G>C	ENSP00000411262.1:n.*1311G>C
ENST00000466883.5:n.2321G>C
NM_000181.3:c.1931G>C	NP_000172.2:p.Cys644Ser
NM_001284290.1:c.1493G>C	NP_001271219.1:p.Cys498Ser
NM_001293104.1:c.1361G>C	NP_001280033.1:p.Cys454Ser
NM_001293105.1:c.1274G>C	NP_001280034.1:p.Cys425Ser
NR_120531.1:n.1977G>C
XM_005250297.3:c.1778G>C	XP_005250354.1:p.Cys593Ser
XM_011516113.1:c.1430G>C	XP_011514415.1:p.Cys477Ser
XM_011516114.1:c.1259G>C	XP_011514416.1:p.Cys420Ser
XM_005250297.4:c.1778G>C	XP_005250354.1:p.Cys593Ser
XM_011516114.2:c.1259G>C	XP_011514416.1:p.Cys420Ser
XM_017012091.1:c.1277G>C	XP_016867580.1:p.Cys426Ser
XM_017012092.1:c.1208G>C	XP_016867581.1:p.Cys403Ser
XM_017012093.2:c.1106G>C	XP_016867582.1:p.Cys369Ser
XR_001744658.2:n.1738G>C
XR_001744659.2:n.1851G>C
XR_001744660.2:n.1783G>C
XR_001744661.2:n.1698G>C
XR_927461.3:n.1936G>C
NM_000181.4:c.1931G>C MANE Select	NP_000172.2:p.Cys644Ser
NM_001284290.2:c.1493G>C	NP_001271219.1:p.Cys498Ser
NM_001293104.2:c.1361G>C	NP_001280033.1:p.Cys454Ser
NM_001293105.2:c.1274G>C	NP_001280034.1:p.Cys425Ser
NR_120531.2:n.1876G>C