Canonical Allele Identifier: CA367637410

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425994T>G (hg19) ; chr7:g.65961007T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65961007T>G , CM000669.2:g.65961007T>G	GRCh38
NC_000007.13:g.65425994T>G , CM000669.1:g.65425994T>G	GRCh37
NC_000007.12:g.65063429T>G	NCBI36
NG_016197.1:g.26308A>C
NG_051954.1:g.92909T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1846A>C MANE Select	ENSP00000302728.4:p.Lys616Gln
ENST00000304895.8:c.1846A>C	ENSP00000302728.4:p.Lys616Gln
ENST00000421103.5:c.1408A>C	ENSP00000391390.1:p.Lys470Gln
ENST00000430730.5:c.*1113A>C	ENSP00000411859.1:n.*1113A>C
ENST00000447929.5:c.*1226A>C	ENSP00000411262.1:n.*1226A>C
ENST00000466883.5:n.2236A>C
NM_000181.3:c.1846A>C	NP_000172.2:p.Lys616Gln
NM_001284290.1:c.1408A>C	NP_001271219.1:p.Lys470Gln
NM_001293104.1:c.1276A>C	NP_001280033.1:p.Lys426Gln
NM_001293105.1:c.1189A>C	NP_001280034.1:p.Lys397Gln
NR_120531.1:n.1892A>C
XM_005250297.3:c.1693A>C	XP_005250354.1:p.Lys565Gln
XM_011516113.1:c.1345A>C	XP_011514415.1:p.Lys449Gln
XM_011516114.1:c.1174A>C	XP_011514416.1:p.Lys392Gln
XM_005250297.4:c.1693A>C	XP_005250354.1:p.Lys565Gln
XM_011516114.2:c.1174A>C	XP_011514416.1:p.Lys392Gln
XM_017012091.1:c.1192A>C	XP_016867580.1:p.Lys398Gln
XM_017012092.1:c.1123A>C	XP_016867581.1:p.Lys375Gln
XM_017012093.2:c.1021A>C	XP_016867582.1:p.Lys341Gln
XR_001744658.2:n.1653A>C
XR_001744659.2:n.1766A>C
XR_001744660.2:n.1698A>C
XR_001744661.2:n.1613A>C
XR_927461.3:n.1851A>C
NM_000181.4:c.1846A>C MANE Select	NP_000172.2:p.Lys616Gln
NM_001284290.2:c.1408A>C	NP_001271219.1:p.Lys470Gln
NM_001293104.2:c.1276A>C	NP_001280033.1:p.Lys426Gln
NM_001293105.2:c.1189A>C	NP_001280034.1:p.Lys397Gln
NR_120531.2:n.1791A>C