Canonical Allele Identifier: CA367637435

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425999T>A (hg19) ; chr7:g.65961012T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65961012T>A , CM000669.2:g.65961012T>A	GRCh38
NC_000007.13:g.65425999T>A , CM000669.1:g.65425999T>A	GRCh37
NC_000007.12:g.65063434T>A	NCBI36
NG_016197.1:g.26303A>T
NG_051954.1:g.92914T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1841A>T MANE Select	ENSP00000302728.4:p.Gln614Leu
ENST00000304895.8:c.1841A>T	ENSP00000302728.4:p.Gln614Leu
ENST00000421103.5:c.1403A>T	ENSP00000391390.1:p.Gln468Leu
ENST00000430730.5:c.*1108A>T	ENSP00000411859.1:n.*1108A>T
ENST00000447929.5:c.*1221A>T	ENSP00000411262.1:n.*1221A>T
ENST00000466883.5:n.2231A>T
NM_000181.3:c.1841A>T	NP_000172.2:p.Gln614Leu
NM_001284290.1:c.1403A>T	NP_001271219.1:p.Gln468Leu
NM_001293104.1:c.1271A>T	NP_001280033.1:p.Gln424Leu
NM_001293105.1:c.1184A>T	NP_001280034.1:p.Gln395Leu
NR_120531.1:n.1887A>T
XM_005250297.3:c.1688A>T	XP_005250354.1:p.Gln563Leu
XM_011516113.1:c.1340A>T	XP_011514415.1:p.Gln447Leu
XM_011516114.1:c.1169A>T	XP_011514416.1:p.Gln390Leu
XM_005250297.4:c.1688A>T	XP_005250354.1:p.Gln563Leu
XM_011516114.2:c.1169A>T	XP_011514416.1:p.Gln390Leu
XM_017012091.1:c.1187A>T	XP_016867580.1:p.Gln396Leu
XM_017012092.1:c.1118A>T	XP_016867581.1:p.Gln373Leu
XM_017012093.2:c.1016A>T	XP_016867582.1:p.Gln339Leu
XR_001744658.2:n.1648A>T
XR_001744659.2:n.1761A>T
XR_001744660.2:n.1693A>T
XR_001744661.2:n.1608A>T
XR_927461.3:n.1846A>T
NM_000181.4:c.1841A>T MANE Select	NP_000172.2:p.Gln614Leu
NM_001284290.2:c.1403A>T	NP_001271219.1:p.Gln468Leu
NM_001293104.2:c.1271A>T	NP_001280033.1:p.Gln424Leu
NM_001293105.2:c.1184A>T	NP_001280034.1:p.Gln395Leu
NR_120531.2:n.1786A>T